Hemorrhoids Clinical Trial
— PEAARSOfficial title:
Pre-Emptive Analgesia in Ano-Rectal Surgery
Verified date | January 2018 |
Source | University of Vermont |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The perianal region is the region around the anus. Administering a pain medication before a
surgery starts is called preemptive analgesia. In some studies, this technique has been shown
to be an effective way to reduce the pain that a patient experiences in the post-operative
timeframe to a greater extent than would be expected simply from the pain medications alone.
One theory of why this occurs suggests that the preemptive analgesia desensitizes brain and
nerves to pain, thereby decreasing the response to painful stimuli, like surgery when they
occur. This leads to a decrease in the amount of narcotic pain medication required after the
procedure, which leads to less side effects and a quicker return to normal functioning. As
perianal surgeries do not usually include a long stay in the hospital, controlling
post-procedure pain is a priority.
The use of preemptive analgesia is in other types of surgeries, such as orthopedics, is well
established, but as the perianal region has not been well studied, its use is not the
standard of care. This type of analgesia uses a combination of medications that are already
in use for post-operative and non-operative pain control and administers them orally prior to
the patient undergoing general anesthesia. The side effects of the medications are the same
as if they had been given after surgery or for non-surgical pain.
The concept of preemptive analgesia is established in other types of surgeries and it has
solid basic science to support its use. The purpose of this randomized, double-blind, placebo
controlled study is to determine if patients undergoing perianal surgeries could benefit from
preemptive pain control. The primary outcome will be whether patients experience less
post-operative pain. Patient post-operative consumption and latency until use of narcotic
pain medication will be the secondary outcomes. The investigators believe that the patients
receiving pain medications before their operation will require less pain medication after
surgery, with minimal increased risk to the patient.
Status | Completed |
Enrollment | 90 |
Est. completion date | May 2017 |
Est. primary completion date | May 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients having anal fistula repairs for anal fistulas recalcitrant to non-surgical management at the University of Vermont Medical Center or Fanny Allen Campuses OR - Patients having anal sphincterotomies for chronic anal fissures recalcitrant to non-surgical management at the University of Vermont Medical Center or Fanny Allen Campuses OR - Patients having hemorrhoidectomies for hemorrhoids recalcitrant to non-surgical management at the University of Vermont Medical Center or Fanny Allen Campuses OR - Patients having anal condyloma excisions for anal condylomas recalcitrant to non-surgical management at the University of Vermont Medical Center or Fanny Allen Campuses - Patients undergoing these surgeries must be American Society of Anesthesiologists (ASA) Physical Status Classification System scores of I (normal, healthy patient), II (patient with mild, systemic disease), or III (patients with more significant disease) Exclusion Criteria: - Allergies to any study medications; - Patient history and chart review for existence of hepatic or renal failure; - Chronic pain syndrome; - Inability to understand or utilize the Numerical Rating Scale (NRS); - Pregnancy; - Patients currently on gabapentin, pregabalin or narcotics - Patients taking chronic steroids, unable to taper off before surgery |
Country | Name | City | State |
---|---|---|---|
United States | University of Vermont Medical Center | Burlington | Vermont |
United States | University of Vermont Medical Center Fanny Allen Campus | Colchester | Vermont |
Lead Sponsor | Collaborator |
---|---|
University of Vermont | American Society of Colon and Rectal Surgeons |
United States,
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* Note: There are 41 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Postoperative pain | Pain will be evaluated using numerical rating scales at specified intervals from the end of surgery up to 7 days postoperatively and mailed back to the investigators. The pain levels will be compared between groups. | End of surgery up to 7 days postoperatively | |
Secondary | Narcotic consumption | Narcotic consumption will be recorded by the subject on medication diaries attached to the respective numerical rating scale. This helps to identify at which time point the patient took a narcotic. This will be compared between groups. | End of surgery up to 7 days postoperatively | |
Secondary | Interval for rescue pain medication | On the aforementioned medication diaries, the patient will record when he or she first needed break through pain medication (i.e. the narcotic prescribed) beyond the scheduled pain medicines. This will help us evaluate the interval between end of the operation and first need for breakthrough pain medication. This number will be compared between groups. | End of surgery up to 7 days postoperatively | |
Secondary | Further pain requirements | By examining the medication diaries, we will be able to evaluate if there were patients who required more than the scheduled pain medications and breakthrough narcotic. This number will be compared between groups. | End of surgery up to 7 days postoperatively |
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