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to study the effect of intra peritoneal levobupivacaine on post operative pain in patients who have undergone Diagnostic laparoscopy

Effect of intra peritoneal levobupivacaine on post laparoscopic pain-Triple blinded randomized control study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/047429
Enrollment
118
Registered
2022-11-18
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Health Condition 1: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system

Interventions

Intervention1: levobupivacaine for first 6hrs,12hrs,24hrs,48hrs after surgery: comparing effectivness of levobupivacaine on post laparoscopy pain for the first 6hrs,12hrs,24hrs,48hrs after surgery Con

Sponsors

rohilkhand medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)ASA risk classification1-2. 2) All women undergoing diagnostic laparoscopic surgery.

Exclusion criteria

Exclusion criteria: 1)ASA >2 2) Wt 3) Contra-indication or previous adverse reaction to bupivacaine

Design outcomes

Primary

MeasureTime frame
main aim of this randomized triple blinded study was to compare post laparoscopic pain in women treated with Levobupivacaine with those treated with 0.9 % sodium chloride Timepoint: 1 year—

Secondary

MeasureTime frame
To compare the efficiency of Intraperitoneal instillation of Levobupivacaine with that of Intraperitoneal instillation of 0.9% sodium chloride in terms of: â?¢ Duration of pain relieving action â?¢ Need of post-operative analgesia â?¢ Quality of post-operative careTimepoint: 1 year—

Countries

India

Contacts

Public ContactDr Nikitha Kotla

Rohilkand Medical college and Hospital

pragya_mshr@yahoo.co.in8435333777

Outcome results

None listed

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