FindTrial
Sign In

Effect of peritoneal local anesthetic plus sedative-analgesics instillation on post-operative pain relief after laparoscopic surgeries.

Comparison of effect of intraperitoneal instillation of additional dexmedetomidine or clonidine along with bupivacaine for post-operative analgesia following laparoscopic cholecystectomy: a prospective, randomized double blind, controlled study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/01/017247
Enrollment
108
Registered
2019-01-25
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K801- Calculus of gallbladder with othercholecystitis

Interventions

Intervention1: Dexmedetomidine: Intraperitoneal Bupivacaine with dexmedetomidine infiltration Control Intervention1: Clonidine: Intraperitoneal Bupivacaine with clonidine infiltration

Sponsors

SVIMS
Lead Sponsor
Sri Venkateswara institute of medical Sciences
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: ï?? Patients undergoing elective laparoscopic cholecystectomy under general anaesthesia. ï?? Patients aged 18-60 years. ï?? Patients of either sex. ï?? Patients coming under American Society of Anesthesiologists physical status I,II,III

Exclusion criteria

Exclusion criteria: ï?? Patients allergic to study drugs. ï?? Patients with acute cholecystitis. ï?? Patients with severe cardiac, pulmonary and renal diseases. ï?? Procedure converted to open cholecystectomy. ï?? Patients in whom abdominal drain is kept. ï?? Patients unwilling to participate in the study. ï?? Patients unable to give informed consent. ï?? Pregnant and lactating women. ï?? Patients who cannot understand or interpret Numerical Rating Scale for pain.

Design outcomes

Primary

MeasureTime frame
a. Magnitude of pain assessed by Numerical Rating Scale.Timepoint: pain within 24 hours at different time intervals.—

Secondary

MeasureTime frame
b. Time to first request of analgesia. c. Analgesic requirement in the first 24 hours post operatively. d. Incidence of shoulder pain in the study groups. e. Adverse effects during the study period. Timepoint: b. Time to first request of analgesia. c. Analgesic requirement in the first 24 hours post operatively. d. Incidence of shoulder pain in the study groups. e. Adverse effects during the study period.—

Countries

India

Contacts

Public ContactALOKA SAMANTARAY

SVIMS

aloksvims@gmail.com9493547653

Outcome results

None listed

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