Pre-incisional ropivacaine plus Diprospan for pain after laparoscopic surgery
Official title: The Efficacy and Safety of Pre-incisional Infiltration With Ropivacaine Plus Diprospan in Patients Undergoing Laparoscopic Surgery: a Multi-center Randomized Controlled Trial.
Run by Beijing Tiantan Hospital · NCT07626463 · Data updated 2026-11-12
This study tests whether injecting ropivacaine with Diprospan before surgery reduces pain after laparoscopic gallbladder, appendix, or hernia operations compared with ropivacaine alone.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 64 Years |
| Sex | All |
| Enrollment | 150 (estimated) |
| Sponsor | Beijing Tiantan Hospital Academic / other |
| Locations | 1 site (Beijing, Beijing Municipality) |
| Status | Recruiting |
| Started | May 30, 2026 |
| Main results expected | May 30, 2027 |
| Study ends | May 30, 2028 |
| Registry record updated | June 17, 2026 |
| Trial ID | NCT07626463 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–64 scheduled for elective laparoscopic cholecystectomy, appendectomy, or hernia repair under general anesthesia, and meeting ASA I–III with ability to consent and comply with follow-up.
✕Probably not a fit
Patients who receive ropivacaine alone or who do not respond to the anti-inflammatory effects may not experience extended analgesia.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional trial compares pre-incisional infiltration of ropivacaine with and without Diprospan in adults undergoing elective laparoscopic cholecystectomy, appendectomy, or hernia repair. The approach targets incision-area inflammation to extend analgesia after surgery. Participants are adults 18–64 with ASA I–III who can consent and comply with follow-up. Primary goals are to see if adding Diprospan can prolong pain relief and improve post-op comfort compared with ropivacaine alone. The study is conducted at Beijing Tiantan Hospital with a lead sponsor from the same institution.
Why it matters
Potential benefit: If successful, patients may experience longer-lasting pain relief after laparoscopic surgery and reduced need for additional analgesics.
How similar studies have gone: Prior work suggests that combining local anesthetics with anti-inflammatory agents can extend analgesia in surgical incisions, though specific combinations and contexts vary.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients scheduled for elective Laparoscopic Surgery for laparoscopic cholecystectomy, appendectomy, or hernia repair under general anesthesia; 2. Ages 18 to 64 years old; 3. American Society of Anesthesiologists (ASA) physical status of I-III; 4. Patients must be able to understand nature and potential personal; consequences of the clinical trial and cooperation with follow-up investigations; 5. signing of the informed consent form. Exclusion Criteria: 1. History of allergies to experimental drugs such as opioids or steroids; 2. Alcohol abuse; Long term use of opioid drugs (exceeding 2 weeks or 3 days per week for more than 1 month); Suspected use of sedatives and analgesics; 3. Use analgesic drugs within 24 hours before surgery; 4. Patients undergoing steroid therapy; 5. Serious neurological disorders, severe liver and kidney dysfunction, heart failure, etc; 6. Unable to use pain assessment scale; 7. Pregnant or lactating patients.
Where it's running
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Beijing Tiantan Hospital
Beijing, Beijing Municipality, China Recruiting
Study contacts
- Study coordinator: Fang Luo
- Email: 13611326978@163.com
- Phone: +86 13611326978
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.