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Comparison of single(adductor canal block) versus two blocks(adductor canal blockand IPACK block) for postoperative analgesia after knee surgery in adult patient.

Randomized study to compare adductor canal block and combination of adductor canal block with ipack block for post operative analgesia in adult patient undergoing knee surgery - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090740
Enrollment
80
Registered
2025-07-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: M239- Unspecified internal derangement of knee

Interventions

Intervention1: Combination of adductor canal block and IPACK block: combine effects of adductor canal block(Inj. bupivacaine 0.125% 10ml)and ipack(Inj. bupivacaine 0.125% 10ml)for postoperative period

Sponsors

Government of gujrat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients willing to consent for the study BMI-18-35 kg/m2 American Society of Anesthesiologist (ASA) Classification I, II, III Elective Knee Surgery under spinal anesthesia

Exclusion criteria

Exclusion criteria: Patients with pre-existing respiratory diseases, cardiac diseases Pregnant patients Patients with history of bleeding disorders or on anticoagulant therapy Patient refusal to participate in study Infection at or near injection site H/O previous knee surgery Allergy to local anesthetics Bilateral knee arthroplasty Patient with neuropathic pain of lower limb

Design outcomes

Primary

MeasureTime frame
POSTOPERATIVE PAIN SCORE EVALUATED BY VRS(VERBAL RATING SCORE) 1.VRS(R)AT REST 2.VRS(M)AT MOVMENTTimepoint: Time from block to be given preoprative to the 24 hours postoperative period.

Secondary

MeasureTime frame
1.Intra operative and post operative hemodynamic monitoring. 2.Post-operative requirement of opioid Analgesic. 3.Incidence of complication related to block(numbness,infection,hematoma). 4.Patient satisfaction score-a verbal neumeric rating scale of patient satisfaction will be obtained in post operative period(no satisfaction/partial satisfaction/complete satisfaction). Timepoint: Time from block to be given preoprative to the 24 hours postoperative period.

Countries

India

Contacts

Public ContactDr Smita R Engineer

B J Medical college Civil hospital

seng_90@yahoo.com9825504948

Outcome results

None listed

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