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A comparison of pain relief: using ropivacaine alone versus ropivacaine with dexmedetomidine in patients undergoing gallbladder removal through keyhole surgery.

A comparative study of postoperative analgesic effect of intraperitoneal instillation of ropivacaine alone and ropivacaine with dexmedetomidine after laparoscopic cholecystectomy. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071224
Enrollment
80
Registered
2024-07-24
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Intraperitoneal instillation of drugs after laparoscopic cholecystectomy: Totally 80 patients in the inclusion criteria undergoing elective laparoscopic cholecystectomy under general

Sponsors

Dr Amitha Anna Sajji
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)ASA Grade I and II Patients 2)Age group of 18-60 years 3)Those patients scheduled for laparoscopic cholecystectomy under general anaesthesia

Exclusion criteria

Exclusion criteria: 1) ASA grade III and IV patients 2) History of allergy to study drugs. 3) cardiac pulmonary hepatic or renal disorders 4) Patient refusal 5) Morbid obese patients 6) Pregnant and lactating females 7) Baseline heart rate less than 50 8)Patients needing conversion to open cholecystectomy will be excluded from the final analysis

Design outcomes

Primary

MeasureTime frame
To assess the intensity of postoperative pain by visual analogue scale in the first 24 hours following intraperitoneal instillation of ropivacaine alone versus ropivacaine plus dexmedetomidine after laparoscopic cholecystectomy.Timepoint: Oh,2h,4h,6h,12h and 24 hour

Secondary

MeasureTime frame
T0 compare the total dose of analgesic used in the first 24 hours between the two groups.Timepoint: 24 hours;To assess the occurrence of any adverse side effects between the two groups.Timepoint: 24 hours;To compare the time to first rescue analgesia between the two groups.Timepoint: 24 hours

Countries

India

Contacts

Public ContactAmitha Anna Sajji

Jubilee Mission Medical College and Research Institute

drmariamt@gmail.com9895266950

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026