Clinical trial Recruiting at 1 site Interventional Ages 18 to 64

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.

More Laparoscopic Cholecystectomy trials

Quick facts

Study typeInterventional
Ages18 Years to 64 Years
SexAll
Enrollment150 (estimated)
SponsorBeijing Tiantan Hospital
Academic / other
Locations1 site (Beijing, Beijing Municipality)
StatusRecruiting
StartedMay 30, 2026
Main results expectedMay 30, 2027
Study endsMay 30, 2028
Registry record updatedJune 17, 2026
Trial IDNCT07626463 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

  • Beijing Tiantan Hospital
    Beijing, Beijing Municipality, China
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.