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New treatment option for Postoperative Bowel Function
Official title Fentanyl vs. Remifentanil in Laparoscopic Cholecystectomy: Effects on Bowel Function and Pain
ClinicalTrials.gov ID: NCT07182097
What this study is testing
What is Fentanyl 2 µg/kg IV bolus + 1-2 µg/kg/h infusion during anesthesia?
Fentanyl 2 µg/kg IV bolus + 1-2 µg/kg/h infusion during anesthesia is an investigational medicine, given as an infusion into a vein, being studied as a potential treatment for postoperative bowel function.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- Background: Postoperative ileus (POI) is a common complication after abdominal surgery, leading to delayed gastrointestinal recovery, prolonged hospitalization, and increased healthcare costs. Opioids, while essential for intraoperative analgesia, are known to impair bowel motility through their μ-receptor effects.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 65
You may be able to join if
- Age 18-65 years
- American Society of Anesthesiologists (ASA) physical status I or II
- Scheduled for elective laparoscopic cholecystectomy
- Provided written informed consent
You likely can't join if
- Opioid use preoperatively
- Previous abdominal surgery
- History of ileus or gastrointestinal disease
- Preoperative electrolyte imbalance
- Liver or renal failure
- Neuromuscular or psychiatric disorders
See the full eligibility criteria
- Age 18-65 years
- American Society of Anesthesiologists (ASA) physical status I or II
- Scheduled for elective laparoscopic cholecystectomy
- Provided written informed consent
- Opioid use preoperatively
- Previous abdominal surgery
- History of ileus or gastrointestinal disease
- Preoperative electrolyte imbalance
- Liver or renal failure
- Neuromuscular or psychiatric disorders
- Known allergy to study medications
- Emergency surgery
- Surgical duration exceeding 90 minutes
The study team makes the final eligibility decision.
Where it's taking place
- Karatay, Konya, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 65 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Karatay, Konya, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.