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Multimodal and Unimodal Analgesia in Cholecystectomy

O

October 6 University

Status and phase

Completed
Phase 2
Phase 1

Conditions

Compare Unimodal and Multimodal Analgesics

Treatments

Drug: Acetaminophen 1 G Oral Tablet
Drug: Celecoxib 400Mg Oral Capsule
Drug: Pregabalin 150mg

Study type

Interventional

Funder types

Other

Identifiers

NCT05547659
FWA00015574

Details and patient eligibility

About

Many surgical procedures are accompanied by postoperative pain with severity moderate, severe or extreme and insufficient postoperative pain control may cause risk of post-surgical complications and risk of chronic post-surgical pain The targets of preoperative pain management are to relieve patient suffering, reduce length of hospital stay and achieve early mobilization after surgery, decreasing opioid consumption and its side effects that are constipation, nausea, vomiting, dizziness, respiratory depression which is the most feared complication being life-threatening and some less common side effects as sedation

Enrollment

95 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing laparoscopic cholecystectomy
  • Patients older than 18 years old

Exclusion criteria

  • Renal or hepatic or cardiac impairment patients
  • Patients with chronic pain history
  • Allergic patients after taking aspirin or other NSAIDs
  • patients with active gastrointestinal bleeding, ulcer and inflammatory bowel diseases or cerebrovascular bleeding

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

95 participants in 3 patient groups

multimodal
Active Comparator group
Description:
pregabalin/ acetaminophen/ celecoxib
Treatment:
Drug: Pregabalin 150mg
Drug: Acetaminophen 1 G Oral Tablet
Drug: Celecoxib 400Mg Oral Capsule
unimodal
Active Comparator group
Description:
Pregabalin
Treatment:
Drug: Pregabalin 150mg
control
No Intervention group

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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