FindTrial
Sign In

A Randomized control study to evaluate the efficacy of of Dual Sub sartorial block in managing post operative pain for total knee arthroplasty

A Randomized control study to evaluate the efficacy of Dual Sub-sartorial Block in managing post operative pain in patients undergoing unilateral Total Knee Replacement. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091612
Enrollment
44
Registered
2025-07-24
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: M179- Osteoarthritis of knee, unspecified

Interventions

Intervention1: USG guided nerve blocks: USG guided dual sub-sartorial block compared with USG guided adductor canal block Intervention2: USG guided nerve blocks for postoperative pain management in pa

Sponsors

Manipal hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA II/III 2. Patients undergoing unilateral total knee replacement 3. Anesthetic management plan of sub arachnoid block

Exclusion criteria

Exclusion criteria: 1. Patient refusal to participate in the study 2. Patient allergic to the Local anesthetic used in the study 3. ASA IV patients 4. Patients undergoing bilateral TKR 5. Anesthetic management plan of General anesthesia

Design outcomes

Primary

MeasureTime frame
To understand the analgesic efficacy of dual sub sartorial block by evaluating the post operative pain score (NRS) and Patient controlled analgesia demands in 2 groups of patients (Adductor canal block and dual sub sartorial block) in patients undergoing total knee replacement surgery under sub arachnoid blockTimepoint: NRS and PCA demands will be compared at 0 hours, 6 hours, 12 hours and 24 hours—

Secondary

MeasureTime frame
1. To assess consumption of rescue analgesia in the 2 aforementioned groups of patients. 2. To assess sensory deficit in the 2 aforementioned groups of patients.Timepoint: 1. Rescue analgesia need will be assessed at baseline, 6 hours, 12 hours & 24 hours. 2. Sensory deficit will be assessed at 6 hours, 12 hours & 24 hours.—

Countries

India

Contacts

Public ContactTejaswini

MANIPAL HOSPITAL OLD AIRPORT ROAD

drniruj@hotmail.com9980758404

Outcome results

None listed

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