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A Study Comparing Two Nerve Block Techniques for Pain Relief After Knee Surgery

Comparison of Motor-Sparing Dual Subsartorial Plexus Block Versus Adductor Canal Block for Postoperative Analgesia in Knee Surgeries: A Randomized Controlled Trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094495
Enrollment
66
Registered
2025-09-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: M233- Other meniscus derangements Health Condition 2: M171- Unilateral primary osteoarthritisof knee

Interventions

Intervention1: GROUP A ? DUAL SUBSARTORIAL BLOCK: GROUP A DUAL SUBSARTORIAL BLOCK WITH 0.2% ROPIVACAINE 15+20ML+ DEXAMETHASONE 4mg Control Intervention1: GROUP B ? ADDUCTOR CANAL BLOCK: ADDUCTOR CA

Sponsors

DR RITU RAJ KUMAR SINGH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients posted for elective knee surgery under spinal and regional anesthesia AGE 18 -70 years. ASA Class I or II BMI 18 to 35 kg/m

Exclusion criteria

Exclusion criteria: Patient refusal. Cognitive and psychiatric illness Contraindication for neuraxial blockade Peripheral neuropathy or neurological deficit Opioid addiction Pregnancy Spinal deformity.

Design outcomes

Primary

MeasureTime frame
To compare the duration of analgesia of the Dual Subsartorial Plexus Block ( Group A)versus the Adductor Canal Block ( Group B ) in patients undergoing knee Arthroscopic surgeriesTimepoint: To compare the duration of analgesia of the Dual Subsartorial Plexus Block ( Group A)versus the Adductor Canal Block ( Group B ) in patients undergoing knee Arthroscopic surgeries

Secondary

MeasureTime frame
1. Comparison of VAS Score between Group A ( Dual Subsartorial block ) and Group B ( Adductor Canal block ). 2. Comparison of hemodynamic parameters like BP, HR, SPO2 for first 24 hours between Group A and Group B. 3. To compare time of first rescue analgesic requirement between the Group A and Group B 4. To assessing Quadriceps muscle strength between the groups 5.Comparison of any complications between the groups . Timepoint: INTRAOPERATIVELY

Countries

India

Contacts

Public ContactDR RITU RAJ KUMAR SINGH

SREE VENKATESHWARA MEDICAL COLLEGE HOSPITAL AND RESEARCH INSTITUTE

rituraj69singh@gmail.com7708359076

Outcome results

None listed

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