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Influence of Intra-abdominal Ropivacaine 0.5% Spray on Postoperative Analgesia in Laparoscopic Surgery.

U

University of Liege

Status

Unknown

Conditions

Pain, Acute

Treatments

Drug: Ropivacaïne 0,5% for appendectomy or cholecystectomy surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT05173090
Ropicoelio

Details and patient eligibility

About

Assessing postoperative pain after ropivacin 0.5% spray in the abdominal cavity during laparoscopic surgery.

Enrollment

120 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Appendectomy or cholecystectomy surgery

Exclusion criteria

  • Allergy to local anesthetics
  • Intolerance to tramadol HCl
  • Patient with peritonitis
  • Pregnant women
  • Surgery without laparoscopy
  • Chronic pain before the operation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

120 participants in 2 patient groups, including a placebo group

Ropivacaïne 0,5%
Active Comparator group
Description:
3 mg/kg of ropivacaine 0.5% sprayed into the abdominal cavity
Treatment:
Drug: Ropivacaïne 0,5% for appendectomy or cholecystectomy surgery
NaCl 0,9%
Placebo Comparator group
Description:
NaCl 0,9% sprayed into the abdominal cavity
Treatment:
Drug: Ropivacaïne 0,5% for appendectomy or cholecystectomy surgery

Trial contacts and locations

0

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Central trial contact

Benjamin Javillier, MD

Data sourced from clinicaltrials.gov

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