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A trial to compare the pain relief provided by two different anaesthetic techniques used ultrasound during keyhole surgery for removal of donorâ??s kidney.

To evaluate the efficacy of USG guided Transversus abdominis plane (TAP ) block analgesia and port site infiltration with ropivcaine and levobupivacaine for laparoscopic donar nephrectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/05/004593
Enrollment
120
Registered
2014-05-13
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: null- ASA I-II,POSTED FOR VOLUNTRY KIDNEY DONATION

Interventions

Intervention1: USG guided TAP block in 60 patients: 20 ml with 2 percent Ropivacaine Control Intervention1: USG guided TAP block in 60 patients: 20 ml with 0.5 percent levobupivacaine

Sponsors

SGPGIMS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All ASA -1,II patient of 18-65 age group who are voluntry kidney donor under GA with laparoscopic donor nephrectomy and who given consent and ready to be part of this study.

Exclusion criteria

Exclusion criteria: obesity, incisions that extended above the umbilicus (hypothesized that the study population had a larger variation in â??surgical insult;â?? that is, some cases involved more organ manipulation and dissection resulting in more visceral pain, for which TAP blocks would be less effective than those for parietal/incisional pain), allergy to drug, failure to give consent, coagulopathy, infection or skin diseases at block site.

Design outcomes

Primary

MeasureTime frame
The important measure of analgesic efficacy in our study will be the duration of action of both analgesics ,requirement of opioid analgesic during the first 24 hrs ,pain scores(NRS).Timepoint: 0 hrs,2 hrs,4,6,8,10,12,24,over a 24 hrs

Secondary

MeasureTime frame
nausea and vomiting, pruritus, hemodynamic stability , patient satisfaction between the two groupsTimepoint: 0 hrs,2 hrs,4,6,8,10,12,24,over a 24 hrs

Countries

India

Contacts

Public ContactDR SANDEEP SAHU

SANJAY GANDHI POSTGRADAUTE INSTITUTE OF MEDICAL SCIENCES,LUCKNOW,UP,INDIA

drsandeepsahu@yahoo.co.in918004904598

Outcome results

None listed

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