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To Compare Post-operative Pain Control Effect Of Ultrasound Guided Two Types Of Field Block Undergoing Arthroscopic Shoulder Surgery.

â??COMPARISON BETWEEN ULTRASOUND GUIDED ANTERIOR SUPRASCAPULAR NERVE BLOCK AND INTERSCALENE NERVE BLOCK FOR POSTOPERATIVE ANALGESIA AFTER ARTHROSCOPIC SHOULDER SURGERYâ??: A PROSPECTIVE RANDOMIZED STUDY.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021596
Enrollment
100
Registered
2019-10-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: O- Medical and Surgical Health Condition 2: S434- Sprain of shoulder joint

Interventions

Intervention1: ULTRASOUND GUIDED INTERSCALENE NERVE BLOCK.: ULTRASOUND GUIDED INTERSCALENE NERVE BLOCK WITH INJECTION ROPIVACAINE 0.25% 10 ML BETWEEN ANTERIOR SCALENE MUSCLE AND MIDDLE SCALENE MUSCLE.

Sponsors

BLK SUPERSPECIALITY HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: PATIENTS WITH ASA GRADE I AND ASA GRADE II, UNDERGOING SHOULDER ARTHROSCOPIC SURGERY.

Exclusion criteria

Exclusion criteria: FOLLOWING PATIENTS WILL BE EXCLUDED FROM STUDY: 1. PATIENTS NOT WILLING TO GIVE CONSENT. 2. RESPIRATORY DISEASE. 3. UNCONTROLLED DIABETES MELLITUS. 4. PATIENTS ON ANTI-COAGULANT AND ANTI-PLATELET DRUGS. 5. PATIENTS ALLERGIC TO LOCAL ANAESTHETIC AND USG GEL. 6. PATIENTS WITH PSYCHIATRIC DRUGS, ALCOHOL AND DRUG ABUSE. 7. PREGNANT PATIENTS 8. PATIENTS WITH ORGAN DYSFUNCTION. 9. PRIOR SURGERY IN NECK OR INFRACLAVICULAR/ SUPRASCAPULAR FOSSA.

Design outcomes

Secondary

MeasureTime frame
1. To study and compare USG guided diaphragmatic movement in the post-operative room in the two groups. 2. To study and compare the forced Vital capacity in the post-operative room. 3. To study and compare the adverse effects, if any, in the two groups. Timepoint: At 2 hours Post-operative- for diaphragmatic movement and forced vital capacity. At 1,2,6,12 and 24 hours for other adverse effects.—

Primary

MeasureTime frame
1. To study and compare Pain score (NRS) at different time interval in the two groups. 2. To study and compare the time required for first rescue analgesia in the two groups. 3. To study and compare the total consumption of Fentanyl in the postoperative period during first 24 hrs measured through Patient Controlled Analgesia (PCA) pump. Timepoint: Post-operative Numeric Rating Scale (0-10) at 1,2,6,12 and 24 hours. Total dose of Injection Fentanyl used in 24 hours.—

Countries

India

Contacts

Public ContactDr Sandeep Dahiya

B L K SUPERSPECIALITY HOSPITAL

drshriprakashsingh@blkhospital.com9810072232

Outcome results

None listed

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