Buprenorphine Transdermal Patches in Arthroscopic Rotator Cuff Repair

Sponsor
Hospital Italiano de Buenos Aires (Other)
Overall Status
Completed
CT.gov ID
NCT03380533
Collaborator
(none)
50
1
2
54.4
0.9

Study Details

Study Description

Brief Summary

Arthroscopic rotator cuff repair is associated with poor post-operative pain management. The multimodal analgesic scheme (oral non-steroidal anti-inflammatory drugs associated with oral opioids) currently used according to the pain management guidelines is insufficient for most of these patients.

There are few reports on the use of buprenorphine in post-operative pain with encouraging results. There is no evidence of its use in the management of post-operative pain of arthroscopic rotator cuff repair

Condition or Disease Intervention/Treatment Phase
Phase 2/Phase 3

Detailed Description

Traditionally, oral opioids have been used to manage the postoperative pain of arthroscopic rotator cuff repair (ARCR) . Due to the intensity of pain, it often requires high doses of opioids, frequently associated with side effects, such as nausea, vomiting, constipation, disorientation, among others, which, in the context of an outpatient, interfere with the postoperative period, sometimes resulting in hospital readmissions. due to both the poor management of pain and the adverse effects of opioids.

Although there are invasive strategies of analgesia, such as the placement of continuous infusion catheters of analgesics in the sub-acromial space, these are methods that demand the management of the devices, in some cases requiring prolongation of hospitalization for the patient. management of the same, without being exempt from complications as any analgesic method added to those related to the method.

Currently, the post-operative analgesia strategy widely accepted globally and that used in our center, is multimodal analgesia, in which NSAIDs (Anti-Inflammatory Non-Steroids) and oral opioids are associated. A combination of both analgesic mechanisms of action is used as a basic scheme, and rescues with opioids are carried out orally. Although the literature supports its cost-benefit, this approach is often insufficient, not achieving adequate control of postoperative pain in ARCR, with 64% of our patients reporting poor pain management in the first week of post-operative and 10% that require re-entry to day hospital for pain management.

The application of transdermal opioid release patches is a method of non-invasive analgesia, which has previously been used with good results for the management of postoperative pain. In ARCR there is no evidence of its use in the management of post-operative pain The main advantages could be related to the plasma stability of the drug (buprenorphine), which implies fewer peaks and valleys of analgesia, a better compliance by the patient since it is of weekly duration and lower incidence of cognitive deterioration related to other opioids.

Compared with other opioids, buprenorphine is associated with a lower risk of abuse, overdose and poisoning due to the ceiling effect. Despite this favorable pharmacological profile, the use of buprenorphine in patches has a lower abuse rate than other forms of administering the same drug. On the one hand, the release rate of the patch may be insufficient to satisfy the compulsive desire and, to that end, the patch may be less desirable. On the other hand, the availability in the market and the way to use the patches could be other conditioning factors.

Study Design

Study Type:
Interventional
Actual Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized Controlled TrialRandomized Controlled Trial
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Treatment
Official Title:
The Use of Buprenorphine Transdermal Patches Improves Post-Operative Pain Management in Arthroscopic Rotator Cuff Repair?
Actual Study Start Date :
Sep 22, 2016
Actual Primary Completion Date :
Dec 8, 2017
Actual Study Completion Date :
Apr 6, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Buprenorphine Patch

Buprenorphine 10mg Patch + Placebo Tablet + Multimodal Oral Scheme Multimodal Oral Scheme: Diclofenac 75mg c 12h Rescues with tramadol 50 mg (maximum rescue dose 150mg, minimum frequency between rescues 4hs)

Drug: Buprenorphine
Buprenorphine 10mg transdermal patch used during the first five postoperative days after arthroscopic rotator cuff repair
Other Names:
  • Buprenorphine Patch
  • Drug: Multimodal Oral Scheme
    Diclofenac 75mg c 12h Tramadol 50mg c 12h. Rescues with tramadol 50 mg (maximum rescue dose 150mg, minimum frequency between rescues 4hs)

    Drug: Placebo Tablet
    Placebo tablet that the patient consumes every 8 hours during the first five days

    Active Comparator: Tramadol Tablet

    Placebo Patch + Tramadol 50mg Tablet + Multimodal Oral Scheme Multimodal Oral Scheme: Diclofenac 75mg c 12h Rescues with tramadol 50 mg (maximum rescue dose 150mg, minimum frequency between rescues 4hs)

    Drug: Placebo Patch
    Adhesive patch with the same macroscopic characteristics to the buprenorphine patch, without drugs.

    Drug: Multimodal Oral Scheme
    Diclofenac 75mg c 12h Tramadol 50mg c 12h. Rescues with tramadol 50 mg (maximum rescue dose 150mg, minimum frequency between rescues 4hs)

    Drug: Tramadol
    Tramadol 50mg tablet that the patient consumes every 8 hours during the first five days
    Other Names:
  • Tramadol Tablet
  • Outcome Measures

    Primary Outcome Measures

    1. Pain perception [Five days]

      subjective perception of pain through the use of an analogous visual scale

    Secondary Outcome Measures

    1. Consumption of rescue opiods [Five Days]

      consumption of rescue opiods

    2. Hours of sleep [5 days]

      hours of sleep

    3. Perception of Sickness [5 days]

      presence or not of nausea

    4. Readmissions rate [5 days]

      record of hospital readmissions for pain or complications related to the use of buprenorphine patches

    5. Misuse or abuse of opioids rate [Fourth month post operatory]

      Behaviors of misuse or abuse of opioids after the immediate postoperative period

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Patient diagnosed with rotator cuff injury, regardless of the type of injury.

    • Patient undergoing Arthroscopic Rotator Cuff Repair

    Exclusion Criteria:
    1. Refusal to participate or inability to understand the informed consent process.

    2. Inability to understand subjective scales of pain

    3. Regular use of narcotics

    4. Allergy or intolerance to drugs used in the protocol

    5. Consumption of drugs that interact with Buprenorphine (anticholinergics, Atropine, Belladonna, Benztropine, Dicyclomine, Diphenhydramine, Isopropamide, Procyclidine and Scopolamine, Antiarrhythmics, Amiodarone, Disopyramide, Dofetilide, Procainamide, Quinidine and Sotalol.

    Anticonvulsants; Carbamazepine, Phenobarbital, Phenytoin and Rifampin)

    1. History of previous surgeries in shoulder treated with RAMR

    2. Previous neuromuscular deficit

    3. Febrile Syndrome

    4. Autoimmune or Rheumatologic Disease

    5. History of intestinal transit disorders (paralytic ileus)

    6. History of alcohol or drug abuse

    7. Patients in psychological or psychiatric treatment for anxiety disorders, personality disorders, mood disorders.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hospital Italiano de Buenos Aires Buenos Aires Caba Argentina 1181

    Sponsors and Collaborators

    • Hospital Italiano de Buenos Aires

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    BERNARDO AGUSTIN BERTONA ALTIERI, MD, Hospital Italiano de Buenos Aires
    ClinicalTrials.gov Identifier:
    NCT03380533
    Other Study ID Numbers:
    • 2960
    First Posted:
    Dec 21, 2017
    Last Update Posted:
    Apr 8, 2021
    Last Verified:
    Apr 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 8, 2021