Comparison of different post surgery pain relieving methods in patients undergoing knee arthroscopic surgeries.

Analgesic effect of adductor canal block with genicular nerve block versus that with infiltration between popliteal artery and posterior capsule of knee in patients undergoing knee arthroscopy: a randomised controlled trial - KneeArB

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/10/058500

Enrollment

Registered

2023-10-11

Start date

Unknown

Completion date

Unknown

Last updated

2025-03-03

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

Conditions

Health Condition 1: S833- Tear of articular cartilage of knee, current

Interventions

Intervention1: ACB with GNB given in pre operative period: Adductor Canal Block with 25 ml of 0.2% ropivacaine and Genicular Nerve Block with 25ml of 0.2% ropivacaine Intervention2: ACB with IPACK giv

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA physical status I / II 2. Both gender 3. Age between 18 to 60 years 4. BMI 20 - 35 kg.m-2 5. Scheduled for knee arthroscopy surgery

Exclusion criteria

Exclusion criteria: 1. Patient’s refusal for the consent 2. Patients having revision knee arthroscopic surgery 3. Inability to understand functioning of VAS 4. Patients not willing for spinal anaesthesia 5. Patients allergic to ropivacaine or study drugs 6. Patients having history of substance abuse 7. Patients with coagulopathy and bleeding disorders 8. Patients having cardiac or renal or hepatic insufficiency 9. Pregnant and Lactating women

Design outcomes

Primary

Measure	Time frame
1. Time to first rescue analgesia after surgeryTimepoint: 1.In PACU at 15 min, 30 min. in WARD at 0h,2 h,4 h,6 h,12 h,18 h,24 h	—

Secondary

Measure	Time frame
1.VAS at rest, VAS on movement 2.Haemodynamics 3. Straight leg raising, range of movements and timed up- and go- 4.Patient satisfaction 5.Adverse effectsTimepoint: 1.Preoperative period, after block at 0min, 5min, 10min, 15min, in PACU for 30 min and in ward for 24h. 2. After block at 0min, 5min, 10min, 15min, intraoperative period, in PACU for 30 min and in ward for 24h. 3.Preoperative period and in ward at 24h. 4.At 24h in ward 5.Preoperative as baseline, immediately after block at 0, 5min, 10min, 15min, in PACU and in ward up to 24h.	—

Measure

Time frame

1.VAS at rest, VAS on movement 2.Haemodynamics 3. Straight leg raising, range of movements and timed up- and go- 4.Patient satisfaction 5.Adverse effectsTimepoint: 1.Preoperative period, after block at 0min, 5min, 10min, 15min, in PACU for 30 min and in ward for 24h. 2. After block at 0min, 5min, 10min, 15min, intraoperative period, in PACU for 30 min and in ward for 24h. 3.Preoperative period and in ward at 24h. 4.At 24h in ward 5.Preoperative as baseline, immediately after block at 0, 5min, 10min, 15min, in PACU and in ward up to 24h.

—

Countries

India

Contacts

Public ContactDr Ramandeep Kaur

Government Medial College and Hospital, Chandiagarh

vanitaanupam@gmail.com9646121649

Outcome results

None listed

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