Pain, Postoperative Clinical Trial
Official title:
Therapeutic Contact Lenses vs. Tight Bandage Patching and Pain Following Pterygium Excision: a Prospective Randomized Controlled Study
This study is designed to determine the most effective post-operative care to relief the patient's discomfort after pterygium excision surgery.
This is a prospective, randomized controlled trial. 50 patients with primary pterygium in
both eyes for whom surgery was advised, will be recruited to the study. Criteria for
pterygium excision surgery is mostly cosmetic, local eye symptoms, or visual impairment.
The following data will be collected and analyzed:
1. Demographic data such as: age, gender
2. Clinical data: best-corrected visual acuity (BCVA) full biomacroscopy examination,
before surgery and at post-operative day (POD) 1 and 3
3. Symptoms and discomfort: Visual Analogue Scale (VAS) score and pain killer use. The
differences in these variables values preoperatively and on the first and 3rd
postoperative day will compared between the two treated eyes.
Surgical technique and postoperative care
All patients will be operated for the same pterygium excision under local anesthesia in the
formal accepted surgical method. All patients will be treated with ofloxacin drops +
dexamethasone drops four times daily during the first postoperative week. The only difference
is that one group will be bandaged with tight bandage patching and the other with therapeutic
contact lenses (TCL) only for the first 24 hours.
Patient-centered outcome
Discomfort and pain will be evaluated on the follow-up meeting on the first and 3rd
postoperative day. The patient will be asked to rate pain and discomfort for each operated
eye on pain scale of VAS ranking the pain on a line from No pain at 0 cm to worst possible
pain at 10 cm and the estimated pain given by the patient's translation of pain into spot on
a line.
Patients will also be queried about the number of hours during which they feel pain, and the
number of pain killers used ( every patient will be given prescription for 3 tabs of
Paracetamol 500 mg (giving no drugs sensitivity for paracetamol) on POD 1 & 3).
Their sleep quality will rated according to whether they reported having a full night's sleep
and the number of times they were awoken due to pain/discomfort.
Statistical analysis
The t test was used to calculate differences in numerical variables (VA, hours of pain,
number of pain killers, etc.). Non-parametric Wilcoxon Mann-Whitney was used to calculate
differences in non-numerical variables such as pain level (VAS scale). Chi-square analyses
were used to calculate proportional group differences (e.g., use of pain killers and sleep
pattern). The overall significance level was set to a value of 0.05. The statistical analysis
was carried out using Microsoft Excel 2013.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05480111 -
The Role of Quadratus Lumborum Blocks Following Minimally Invasive Hysterectomy
|
Phase 4 | |
Completed |
NCT06129305 -
Erector Spina Muscle Distance From the Skin at Different Thoracal Elevations
|
||
Completed |
NCT04401826 -
Micro-surgical Treatment of Gummy Smile
|
N/A | |
Recruiting |
NCT04020133 -
the Role of Popliteal Plexus Block in Pain Management After Anterior Cruciate Ligament Reconstruction.
|
N/A | |
Completed |
NCT03023462 -
Efficacy of an Anterior Quadratus Lumborum Block vs. a TAP-block for Inguinal Hernia Repair
|
N/A | |
Completed |
NCT03546738 -
Spinal Cord Burst Stimulation for Chronic Radicular Pain Following Lumbar Spine Surgery
|
N/A | |
Completed |
NCT03652103 -
Efficiency of Erector Spinae Plane Block For Patients Undergoing Percutaneous Nephrolithotomy
|
Phase 4 | |
Terminated |
NCT03261193 -
ITM + Bupivacaine QLB vs. ITM + Sham Saline QLB for Cesarean Delivery Pain
|
Phase 3 | |
Withdrawn |
NCT03528343 -
Narcotic vs. Non-narcotic Pain Regimens After Pediatric Appendectomy
|
Phase 1/Phase 2 | |
Completed |
NCT02525133 -
Phase 3 Study of Efficacy and Safety of the XaraColl® Bupivacaine Implant After Hernioplasty
|
Phase 3 | |
Completed |
NCT03244540 -
Regional Analgesia After Cesarean Section
|
Phase 4 | |
Enrolling by invitation |
NCT05316168 -
Post Operative Pain Management for ACL Reconstruction
|
Phase 3 | |
Recruiting |
NCT04130464 -
Intraperitoneal Infusion of Analgesic for Postoperative Pain Management
|
Phase 4 | |
Enrolling by invitation |
NCT04574791 -
Addition of Muscle Relaxants in a Multimodal Analgesic Regimen for Analgesia After Primary Total Knee Arthroplasty
|
N/A | |
Completed |
NCT04526236 -
Influence of Aging on Perioperative Methadone Dosing
|
Phase 4 | |
Completed |
NCT04073069 -
Scalp Infiltration With Diprospan Plus Ropivacaine for Postoperative Pain After Craniotomy in Adults
|
Phase 4 | |
Recruiting |
NCT05351229 -
Intrathecal Morphine for Analgesia in Video-assisted Thoracic Surgery
|
Phase 4 | |
Enrolling by invitation |
NCT05543109 -
Ultrasound Guided Psoas Compartment Block vs Suprainguinal Fascia Iliaca Compartment Block
|
N/A | |
Completed |
NCT05346588 -
THRIVE Feasibility Trial
|
Phase 3 | |
Completed |
NCT04919317 -
Combination Dexamethasone and Bupivacaine Pain Control in Reduction Mammaplasty
|
Phase 2 |