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A Study To Compare The Transversus Abdominis Plane Block and Erector Spinae Plane Block in Minimally Invasive Nephrectomy Surgeries

A Randomoised,Prospective, Double Blinded Study To Compare The Efficacy Of Ultrasound Guided Transversus Abdominis Plane Block and Erector Spinae Plane Block in Minimally Invasive Nephrectomy Surgeries - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092850
Enrollment
50
Registered
2025-08-12
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: C649- Malignant neoplasm of unspecifiedkidney, except renal pelvis

Interventions

Intervention1: ERECTOR SPINAE PLANE BLOCK: To compare The Efficacy of Erector Spinae Plane Block In Minimally Invasive Nephrectomy Surgeries Intervention2: Nil: Nil Intervention3: Transversus Abdomini

Sponsors

SRM Institutes For Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)ASA grade 1 and 2,Any gender ,Age 20 to 70 years ,BMI 18 to 30 ,Patients willing to participate in the study ,Patients admitted for minimally invasive nephrectomy surgery ,No history of allergy to Local anaesthetics

Exclusion criteria

Exclusion criteria: 1)ASA grade 3, 4, 5,Pregnant and lactating mother,Age less than 20 years and more than 70 years,Obese individuals with BMI more than 30,Chronic history of Opioid abuse,History of allergy to Local anaesthetics,Patients not willing to participate in this study

Design outcomes

Primary

MeasureTime frame
1)To observe intraoperative Remifentanil requirement and the pain score using Visual Analog Scale (VAS) score for first 24 hours,postoperative Tramadol requirement for first 24 hoursTimepoint: 12 months

Secondary

MeasureTime frame
1) To observe the incidence of hemodynamic disturbances during perioperative period 2) To observe the incidence of side effects of opioids such as postoperative nausea, vomiting, sedation and respiratory depression Timepoint: 12 months

Countries

India

Contacts

Public Contactshanmugapriya g

SRM INSTITUTES FOR MEDICAL SCIENCES

anaes1879@yahoo.com9790930134

Outcome results

None listed

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