NCT06688643Completed
The Impact of Intrathecal Morphine Versus Continuous Epidural Analgesia on Return of Bowel Function in Patients Undergoing Laparoscopic Ileal Conduit
The Impact of Intrathecal Morphine Versus Continuous Epidural Analgesia on Return of Bowel Function in Patients Undergoing Laparoscopic Ileal Conduit : a Prospective, Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 14 Nov 2024
Brief summary (registry, in English)
This study aims to compare the effects of intrathecal morphine (ITM) and continuous epidural analgesia (CEA) on bowel function recovery after Bricker surgery.This study was a prospective, randomized controlled trial that included 72 patients with bladder cancer undergoing elective Bricker surgery, who were randomly assigned to either the ITM group (n=36) or the CEA group (n=36). Postoperatively, patients in both groups received either ITM or CEA for pain management, and postoperative bowel function recovery time, pain scores, PONV, itching, and other indicators were recorded.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 58 (actual)
- First submitted
- 11 Nov 2024
- Start date
- 25 Jan 2022
- Primary completion date
- 1 Nov 2024
- Lead sponsor
- Xiaguang Duan
- Diseases
- Bladder cancer, Childhood cancers
- NCT number
- NCT06688643
What you commit to
- Study type: Interventional
- Participants enrolled: 58
- From 25 Jan 2022 to the primary completion date, 1 Nov 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.
Other illness
- allergies to any anesthetic agents used in this study
- hypersensitivity to pain
- a history of gastrointestinal disease
- sleep disorders
Other
- refused to sign the consent form
- uncooperative were deemed ineligible for clinical evaluation
Who the study is looking for
- All participants provided informed consent voluntarily
- ASA I-III
Sex: All · Does not accept 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 |
|---|---|---|---|
| Inner Mongolia Baogang Hospital Coordinator of this site? Confirm its status | Baotou | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.