NCT04240626CompletedPhase 4
Multimodal Analgesia Effect on Post Surgical Patient
Source: ClinicalTrials.gov · Last updated 14 Sept 2026
Brief summary (registry, in English)
Patients undergoing Bariatric Surgery at the University of California Davis Medical Center will be divided into two groups, one receiving Standard of Care pain control medications vs the second group which will receive non-narcotic pain medications with rescue pain medications available if needed
- Status (registry)
- Completed
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 60 (actual)
- First submitted
- 16 Oct 2019
- Start date
- 20 Jan 2021
- Primary completion date
- 24 Jun 2025
- Lead sponsor
- University of California, Davis
- Diseases
- Obesity
- NCT number
- NCT04240626
What you commit to
- Study type: Interventional · Phase 4
- Participants enrolled: 60
- From 20 Jan 2021 to the primary completion date, 24 Jun 2025
- 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
- Not having an index weight los surgery for obesity
- Do not meet the NIH Standards for weight loss surgery
- Additional planned or unplanned procedures during the index surgical procedure such as Cholecystectomy or extensive lysis of adhesions (\>30 minutes)
Other illness
- A history of open abdominal surgery including umbilical, ventral, or splengalic hernia repair with or without mesh implantation, transplant or vascular surgery or any foregut procedures including hiatal hernia repair or anti-reflux surgery
- Arthritis, Fibromyalgia, chronic pain syndrome
- Other conditions requiring daily use of oral pain medications
- Allergy to Gabapentin
Age
- Patients less than 35 years of age or older than 65 years of age at the time of surgical consent
Other
- BMI \< 30
- Men
- Women considering or currently planning on gender altering/modification
- ASA score of 4 or higher
- Prisoners
Who the study is looking for
- Women who undergo index weight loss procedures at UC Davis Medical Center
- Women with a BMI =\>30
- Age from 35-65
- American Society of Anesthesiology (ASA) score of 3 or less
- No previous history of prior abdominal/foregut surgery
Age in the registry: 35 years to 65 years · Sex: Female · 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 |
|---|---|---|---|
| UC Davis Health Coordinator of this site? Confirm its status | Sacramento | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.