NCT05560230CompletedPhase 4
Intraoperative Clonidine for Postoperative Pain Management in Patients Undergoing Surgical Treatment for Endometriosis
Intraoperative Clonidine for Postoperative Pain Management in Patients Undergoing Surgical Treatment for Endometriosis: a Prospective, Double-blind, Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 23 Aug 2024
Brief summary (registry, in English)
The role of a single dose of intraoperative clonidine on postoperative opioid requirements, pain intensity and opioid-related side effects in patients undergoing surgical treatment for endometriosis remains scarcely explored. A prospective double-blind, randomised controlled trial investigating the effect of a single-dose of intraoperative clonidine in patients undergoing surgical treatment for endometriosis is therefore conducted.
- Status (registry)
- Completed
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 120 (actual)
- First submitted
- 26 Sept 2022
- Start date
- 3 Oct 2022
- Primary completion date
- 13 Aug 2024
- Lead sponsor
- University of Aarhus
- Diseases
- Endometriosis
- NCT number
- NCT05560230
What you commit to
- Study type: Interventional · Phase 4
- Participants enrolled: 120
- From 3 Oct 2022 to the primary completion date, 13 Aug 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Daily opioid consumption the last 7 days before surgery
Other illness
- Allergy to clonidine
- Known severe renal insufficiency
Age
- Age \< 18 years
Other
- American Society of Anesthesiologists (ASA) physical status IV or V
- Inability to provide informed consent
- Known severe bradyarrhythmia
- Pregnancy, lactation:
- Pain intensity \>5 on more than half of the days during the last month
Who the study is looking for
- Patients scheduled for surgical laparoscopic treatment of endometriosis at Aarhus University Hospital
Age in the registry: 18 years to 110 years · Sex: Female · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Aarhus University Hospital Coordinator of this site? Confirm its status | Aarhus | Denmark | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.