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TWO BLOCKS COMPARISION FOR ANALGESIA IN TOTAL KNEE REPLACEMENT.

A Tale of Two Blocks: Comparing Adductor Canal and Dual Subsartorial techniques in Total Knee Replacement. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100451
Enrollment
60
Registered
2026-01-07
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: M171- Unilateral primary osteoarthritisof knee

Interventions

Intervention1: DUAL SUBSARTORIAL BLOCK: DUAL SUBSARTORIAL BLOCK IN TOTAL KNEE REPLACEMENT IN UNILATERAL KNEE WITH DRUG FORMULATION AS 35ml OF TOTAL DRUG VOLUME WAS PREPARED WITH A CONCENTRATION OF 0

Sponsors

MMI NARAYANA SUPERSPECIALITY HOSPITAL , RAIPUR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of age 18-75 years of ASA I and II Physical Classes, posted for Total Knee Replacement.

Exclusion criteria

Exclusion criteria: Age less than 18 and more than 75, ASA III and IV, Infection at injection site, Pregnancy, lactating mother, Patient with psychological, neurological or coagulation disorder, History of allergy to local anaesthetics or drugs used in the study.

Design outcomes

Primary

MeasureTime frame
PRIMARY OBJECTIVE: 1) Duration of post-operative analgesia. 2) Total dose of rescue analgesic required in first 24 hours. 3) VAS (Visual Analog Scale) score at 2, 4, 6, 12 and 24 hours post-operatively. 4) Motor performance and Range of movement in the knee joint in post operative period. Timepoint: *RESCUE ANALGESIA IN FIRST 24HOURS * VAS (Visual Analog Scale) score for pain at 2, 4, 6, 12 and 24 hours post-operatively. *Motor performance and Range of movement in the knee joit--WITHIN 24 HOURS.

Secondary

MeasureTime frame
SECONDARY OBJECTIVE: 1) To analyse the incidences of complications, if any, associated with Adductor Canal Block, Dual Subsartorial Block & Pre Anesthesia Checkup 2) To assess the side effects of drugs used in the studyTimepoint: Both the outcomes at 5 minutes 10 minutes 15 minutes 30 minutes 60 minutes & 120 minutes minutes regularly after the intervention done.

Countries

India

Contacts

Public ContactMANISH CHOUBEY

MMI NARAYANA SUPERSPECIALITY HOSPITAL,RAIPUR

arunandappan@gmail.com9584411011

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026