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Comparison between intraperitoneal ropivacaine alone and with Dexmedetomidine in laproscopic cholecystectomy

A comparative evaluation of intraperitoneal instillation of ropivacaine alone or with dexmedetomidine for postoperative analgesia following laproscopic cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/03/017963
Enrollment
80
Registered
2019-03-07
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: O- Medical and Surgical

Interventions

Intervention1: Intraperitoneal instillation of drug following laproscopic cholecystectomy: For postoperative analgesia Control Intervention1: Ropivacaine alone and with Dexmedetomidine: For duration o

Sponsors

Jln medical college Ajmer
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age group between 18 years to 60 years of both sex undergoing laparascopic cholecystectomy. 2.Patients belonging to ASA (American Society of Anaesthesiologists) grade-I and grade-II. 3.Gall Bladder calculi or polyp with no evidence of acute cholecystitis at the time of surgery.

Exclusion criteria

Exclusion criteria: 1.Age less than 18 year of age or more than 60 year of age 2.ASA grade III or more (American Society of Anaesthesiology) 3.Pregnancy 4.Acute Cholecystitis 5.Choledocolithiasis 6.Conversion of laparascopic cholecystectomy to open cholecystectomy. 7.patient who are allergic study drug,severe cardiac disease ,pulmonary disease, neurological disease patients in whom abdominal drain was put

Design outcomes

Primary

MeasureTime frame
The intensity of postâ??operative pain was recorded for all the cases using VAS score after surgery Comaprison of effect in the patients between ropivacine alone and ropivacine with dexmedetomidineTimepoint: Duration of the study is around 1 year

Secondary

MeasureTime frame
Total amount of rescue analgesic in 24 hours Haemodynamic change Any side effectsTimepoint: Duration of study around 1 year.

Countries

India

Contacts

Public ContactDr Veena mathur

J.L.N. medical college ajmer

veenamathur41@gmail.com

Outcome results

None listed

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