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STUDY REGARDING PAIN RELIEF IN POSTOPERATIVE MINIMAL INVASIVE SURGERY FOR KIDNEY REMOVAL FOR KIDNEY TRANSPLANTATION FOLLOWING INTRAPERITONEAL NEBULIZATION AND INTRAPERITONEAL INSTILLATION OF ROPIVACAINE

INTRAPERITONEAL NEBULIZATION VERSUS INTRAPERITONEAL INSTILLATION OF ROPIVACAINE FOR POST-OPERATIVE PAIN MANAGEMENT FOLLOWING LAPROSCOPIC DONOR NEPHRECTOMY

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/08/004926
Enrollment
60
Registered
2014-08-25
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: null- ASA-I and II

Interventions

Intervention1: Experimental
Nebulization: Drug
Ropivacaine 60 mg nebulization group will receive intraperitoneal nebulization of ropivacaine 1%, 3 ml before the start of renal dissection and again at the end of surgery just before deflation of pne
Instillation: Drug
Ropivacaine 100mg Instillation group will receive 0.5%, 20 ml on kidney after induction of pneumoperitoneum but before dissection of kidney

Sponsors

SGPGIMS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA-I-II Scheduled for laparoscopic Nephrectomy Free from pain in preoperative period Not using analgesic drugs before surgery Without cognitive impairment or mental retardation written informed consent

Exclusion criteria

Exclusion criteria: Patient under 18 or over 65 years ASA III,IV or V Emergency or urgency surgery Postoperative admission in an intesive care unit Severe hepatic or renal impairment Pregnancy or lactation Allergy to one of the specific drugs under study Alcohol or drug addiction Acute infection or chronic disease Progressive degenerative disease of CNS Seizures or chronic therapy with antiepileptic drugs Cognitive impairment or mental retardation Any type of communication problem No written informed consent

Design outcomes

Primary

MeasureTime frame
Postoperative painTimepoint: In PACU, At 6 hr,at 24 hr,at 48 hr and at the time of discharge

Secondary

MeasureTime frame
Hospital morbidityTimepoint: Intraoperative and Postoperative;Hospital stayTimepoint: Time in hours elapsed between surgery and hospital discharge;Postoperative Fentanyl requirementTimepoint: In PACU,At 6 hr,at 24 hr,48 hr,at the time of discharge;Quality of life after surgeryTimepoint: 4 weeks after surgery;Time of Unassisted walkingTimepoint: Time in hours between PACU discharge and when the patient able to walk

Countries

India

Contacts

Public ContactDr Anil Agarwal

Sanjay Gandhi Postgraduate Institute of Medical Sciences

anil_sgpgi@hotmail.com08004904589

Outcome results

None listed

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