NCT06182111 Intraoperative Administration of Intravenous Morphine in Patients Undergoing Laparoscopic Cholecystectomy
| NCT ID | NCT06182111 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Esbjerg Hospital - University Hospital of Southern Denmark |
| Condition | Postoperative Pain |
| Study Type | OBSERVATIONAL |
| Enrollment | 300 participants |
| Start Date | 2024-06-01 |
| Primary Completion | 2025-05-31 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 300 participants in total. It began in 2024-06-01 with a primary completion date of 2025-05-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The goal of this observational, quality improvement study is to compare the effect of a dose of morphine given during gall-bladder removal surgery. The main questions to answer are: * Do participants, who are given given a dose of morphine during gall-bladder removal surgery, experience less pain after surgery? * Does a dose of morphine during gall-bladder removal surgery cause more side effects? The investigators will compare the effects of two types of anesthesia: a) anesthesia without morphine during surgery, and b) anesthesia with morphine during surgery.
Eligibility Criteria
Inclusion Criteria: * patients who have had elective laparoscopic cholecystectomy/planned gall-bladder removal surgery Exclusion Criteria: * age limit as above * patients unable to give consent to anesthesia * patients unable to participate in pain scoring * patients with chronic pain syndromes, characterized by patients receiving regular analgesic treatment and patients with active or previous contact to pain clinic) * patients with active or previous substance abuse * emergency surgery
Contact & Investigator
Sanne V Nielsen, MD
PRINCIPAL INVESTIGATOR
Esbjerg Hospital - University Hospital of Southern Denmark
Frequently Asked Questions
Who can join the NCT06182111 clinical trial?
This trial is open to participants of all sexes, aged 21 Years or older, studying Postoperative Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06182111 currently recruiting?
Yes, NCT06182111 is actively recruiting participants. Contact the research team at sanne.vibe.nielsen@rsyd.dk for enrollment information.
Where is the NCT06182111 trial being conducted?
This trial is being conducted at Esbjerg, Denmark.
Who is sponsoring the NCT06182111 clinical trial?
NCT06182111 is sponsored by Esbjerg Hospital - University Hospital of Southern Denmark. The principal investigator is Sanne V Nielsen, MD at Esbjerg Hospital - University Hospital of Southern Denmark. The trial plans to enroll 300 participants.