Pain Clinical Trial
Official title:
Chronic Significant Pain and Functional Outcome After Laparoscopic Versus Open Groin Hernia Mesh Repair: Design of a Randomized Controlled Clinical Trial
Background: Large acceptance of mesh reinforcement techniques in groin hernia repair lowered
recurrence rates for all techniques. Recurrence rate alone is not the main quality criterion
for hernia repair anymore. Chronic significant post operative pain is a common, clinically
relevant, poorly understood and poorly studied entity which is 3 to 5 times more common than
hernia recurrence. As a subgroup to chronic significant post operative pain or as a separate
entity, sexual dysfunction due to ejaculatory and genital pain after inguinal hernia repair
may happen in approximately 2.5% of patients. Patient's preoperative psychological profile
as well as pain exposure history is showed to be important in the development of chronic
significant post operative pain. The objective of this study is to analyse chronic
significant post operative pain and the functional outcome status of patients after
laparoscopic repair compared to open repair.
Methods: A randomized controlled non-blinded clinical trial is designed to compare open
inguinal hernia mesh repair with laparoscopic totally extraperitoneal repair on chronic
significant post operative pain, pain related sexual function disorders, complications,
health related quality of life outcomes, recurrence rates, and cost. Volunteers will be
recruited in Geneva University Hospital, department of surgery, visceral surgery unit.
Eligibility criteria is male patient aged over 21 years, with reducible inguinal unilateral
or bilateral primary hernia who are candidates for elective surgery and medically fit for
general anesthesia.130 patients will be enrolled for each group to achieve an α-Level of
0.05 and a power of 80%. Follow-up will take place at 10th, 30th days as well as 3 12 and 24
post operative months by questionnaires and by clinical exam by independent expert. An
overall cost-analysis will be realized. Patient enrollment in the study will start in April
2008 and estimated to end in may 2009.
Hernia repair is the most frequent elective operation performed in general surgery. Chronic
pain or persistent neuralgia has been recognized as a complication after inguinal hernia
repair but was reported in the 1980s as a rare and infrequent condition. Studies from the
mid 1990s have reported a higher frequency, with up to 50% of patients reporting pain after
hernia repair more than 1 year after surgery. Chronic pain after hernia repair can be
disabling, with considerable impact on quality of life. The natural history of postoperative
pain, including its prevalence, etiology, duration, associated disability and it's social
and economical impact remain undefined.
The Cooperative Hernia Study (1996) assessing postoperative pain in a prospective trial
including 315 open non-mesh repair patients with 2 years follow-up found at 1 year, 62.9% of
groin or inguinal pain and 11.9% of patients had moderate to severe pain; 53.6% had pain and
10.6% of patients continued to report moderate to severe pain 2 years postoperatively.
In a prospective consecutive case series study of 500 consecutive operations in 466
unselected adult patients for open groin hernia repair in Denmark (1994-1996), 1 year after
surgery, 19% of patients had some degree of pain, 6% had moderate or severe pain. Pain
restricted daily function 6% of patients.
A cross-sectional cohort study based on the Danish Hernia Database (1998) to determine the
incidence of groin pain 1 year after inguinal hernia repair and to assess the influence of
chronic groin pain on function, detected 28.7% of pain in the groin area and 11.0% of the
patients reported that pain was interfering with work or leisure activity. There were no
difference in the incidence of pain with regard to the different types of hernia, the
different types of surgical repairs, or the different types of anesthesia.
A questionnaire survey of a historical cohort of 351 patients who underwent inguinal hernia
surgery in Aberdeen - Scotland (1995-1997) reported 30% chronic pain. Character of this pain
was predominantly neuropathic.
Definition of chronic pain The definition of "chronic pain" by the International Association
of the Study of Pain is "pain lasting for 3 months or more". There is no consensus on
neither in the definition, nor the severity grades of CSPOP in the literature. In the
Cooperative Hernia Study, Cunningham et al. clearly described mild, moderate, and severe
pain. Mild pain was defined as an occasional pain or discomfort that did not limit activity,
with a return to lifestyle before hernia; moderate pain, as pain preventing return to normal
preoperative activities (i.e., inability to continue with activities before hernia such as
golf, tennis, or other sports, and inability to lift objects without pain, that patients had
been lifting before the hernia occurrence); and severe pain, as pain that incapacitated the
patient at frequent intervals or interfered with activities of daily living (i.e., a pain
constantly present, or intermittently present but so severe as to impair normal activities,
such as walking). Other studies defined chronic pain as "that persisting for one year
postoperatively". One Dutch study defined pain as pain in the groin or scrotum lasting more
than 1 month after surgery. In our study chronic pain is defined as a minimal score > 4
using the quadruple visual analogue scale (VASQ) 3 months after procedure.
Characteristics and etiology of chronic pain Somatic, neuropathic, and visceral chronic pain
syndromes are described. Cunningham et al. reported the somatic pain syndrome as the most
common type of chronic post hernia pain. The pain is localized to common ligamentous
insertion to the pubic tubercle. Somatic pain may be due to the damage to the pubic tubercle
during the stapling of mesh prosthesis or from deep muscle layers. Incorporation of the
periosteum of the pubic tubercle into the most medial suture during open hernia repair is
accused. Neuropathic pain is probably attributable to damage to the ilioinguinal or
genitofemoral nerve. Neuropathic pain usually develops in the sensory distribution of an
injured nerve. Chronic residual neuralgia occurs as a result of surgical handing of sensory
nerves. The nerve trauma can be due to partial or complete division, stretching, contusion,
crushing, electrical damage, or sutures compression. Secondary nerve damage can occur due to
irritation or compression by an adjacent inflammatory process such as granuloma. Neuropathic
pain described as pulling, tugging, tearing, throbbing, stabbing, shooting, numbing, and
dull. The onset of neuropathic pain is often delayed, occurring after a latent period of
days to weeks. Pain is often aggravated by ambulation, stooping or hyperextension of hip and
sexual intercourse; and alleviated by recumbent position and flexion of the hip and thigh.
In laparoscopic hernia repair when stapling the mesh, it can penetrate the wall of the
inguinal canal entrapping and irritating the sensory nerves. Kinking of the nerves may cause
chronic irritation. The third pain syndrome described in the literature is visceral. For
example, pain encountered only on ejaculation due to dysfunction of periurethral structures
involved in ejaculation. One possible mechanism is the injury to either somatic sacral or
sympathetic nerves, resulting in dyssynergia of the ejaculatory effector muscles. It can
also be due to stricture in the spermatic duct from the scar tissue or twisting of the cord.
Prognosis of chronic pain Once chronic pain is installed, it does not change without a
radical treatment. Cunningham et al. reported a prevalence of mild, moderate, or severe pain
of 63% at 1 year postoperatively, which was reduced to 54% after 2 years. Those patients who
reported moderate to severe pain at 1 year (12%) continued to report persistent pain at 2
years (11 %).
Risk of developing chronic pain
- Predisposing psychological factors Preoperative psychological state of patient
(Depression, dependencies, drug consumption etc.) or history of chronic pain with
previous surgery or accident may be a predicting factor.
- Surgical factors Recurrent hernia, preoperative pain and absence of visible bulge
before surgery, delayed onset of symptoms after surgery, high pain scores at one week
postoperatively and requirement of four or more weeks before returning to work are
reported as risk factors for developing of chronic pain.
Impact of surgical technique Several different surgical techniques are studied with each
other in the literature and different meta analyses, each with different point of interest,
gives different lectures of the reality. Despite the fact that there is no consensus in the
literature, surgical technique is clearly one of the key parameters. The overall frequency
of chronic pain is higher in studies with specific measurements, where pain is the primary
outcome of interest.
- OMR vs. non-mesh repair The hypothetical advantage of tension free repair on chronic
pain issue is not confirmed. Two retrospective cohort studies coming from the tenors of
open mesh repair, reported less chronic pain with mesh repair. This advantage of mesh
repair on pain scores versus conventional no-mesh repairs is not confirmed by
randomized controlled trials.
- LR vs. OMR The only study comparing laparoscopic totally extraperitoneal (TEP) repair
(Polypropylene mesh without fixation) with classic OMR (Lichtenstein) comes from Kumar
et al. They find overall 30% of "chronic pain and discomfort" (22,5% for LR, 38,3% for
OMR) after a mean of 21 months post hernia repair. Medical Research Council trial
reported a significantly higher incidence of chronic pain after open repair than after
laparoscopic repair (37 % versus 29 %) at 1 year. This trial, however, included
non-mesh repairs in the open group and transabdominal preperitoneal (TAP) and TEP
repairs in the laparoscopic group. In a meta-analysis of randomized controlled trials
of laparoscopic and open prosthetic mesh repair of groin hernia, EU Trialists found
that chronic pain is less likely to occur after laparoscopic repair than after open
repair.
- TEP or TAP? The TAP repair is historically the technique of choice in the north
america. Most of the literature compares TAP to another technique. In this technique,
flat, heavy weighted polypropylene meshes were used and fixed with staplers or tackers.
Peritoneal tears were also closed with the same technique. Higher rates of chronic pain
were reported after TAP repair versus TEP repair. Nerve entrapment during these several
stapling procedures was probably the main reason. TAP is also strongly associated to
"rare but serious vascular and visceral complications". The Medical Research Council
trial reported that all serious complications occurred in patients undergoing the TAP
approach. Most of the postoperative complications as sepsis on bowel fistula with mesh,
mechanical ileus on adherences or port site hernias are seen in TAP repair. In our
practice TEP repair is the technique of choice. Dissection is realized without the use
of balloon dissector, an anatomic, preformed anatomic polyester mesh implanted without
fixation by stapling, tacking or suture.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT05559255 -
Changes in Pain, Spasticity, and Quality of Life After Use of Counterstrain Treatment in Individuals With SCI
|
N/A | |
Completed |
NCT04748367 -
Leveraging on Immersive Virtual Reality to Reduce Pain and Anxiety in Children During Immunization in Primary Care
|
N/A | |
Terminated |
NCT04356352 -
Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain
|
Phase 2/Phase 3 | |
Completed |
NCT05057988 -
Virtual Empowered Relief for Chronic Pain
|
N/A | |
Completed |
NCT04466111 -
Observational, Post Market Study in Treating Chronic Upper Extremity Limb Pain
|
||
Recruiting |
NCT06206252 -
Can Medical Cannabis Affect Opioid Use?
|
||
Completed |
NCT05868122 -
A Study to Evaluate a Fixed Combination of Acetaminophen/Naproxen Sodium in Acute Postoperative Pain Following Bunionectomy
|
Phase 3 | |
Active, not recruiting |
NCT05006976 -
A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study
|
N/A | |
Completed |
NCT03273114 -
Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain
|
N/A | |
Enrolling by invitation |
NCT06087432 -
Is PNF Application Effective on Temporomandibular Dysfunction
|
N/A | |
Completed |
NCT05508594 -
Efficacy and Pharmacokinetic-Pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001
|
Phase 2/Phase 3 | |
Recruiting |
NCT03646955 -
Partial Breast Versus no Irradiation for Women With Early Breast Cancer
|
N/A | |
Active, not recruiting |
NCT03472300 -
Prevalence of Self-disclosed Knee Trouble and Use of Treatments Among Elderly Individuals
|
||
Completed |
NCT03678168 -
A Comparison Between Conventional Throat Packs and Pharyngeal Placement of Tampons in Rhinology Surgeries
|
N/A | |
Completed |
NCT03931772 -
Online Automated Self-Hypnosis Program
|
N/A | |
Completed |
NCT03286543 -
Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System
|
N/A | |
Completed |
NCT02913027 -
Can We Improve the Comfort of Pelvic Exams?
|
N/A | |
Terminated |
NCT02181387 -
Acetaminophen Use in Labor - Does Use of Acetaminophen Reduce Neuraxial Analgesic Drug Requirement During Labor?
|
Phase 4 | |
Recruiting |
NCT06032559 -
Implementation and Effectiveness of Mindfulness Oriented Recovery Enhancement as an Adjunct to Methadone Treatment
|
Phase 3 | |
Active, not recruiting |
NCT03613155 -
Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care
|