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REDUCTION IN REQUIREMENT OF POST OPERATIVE PAIN MEDICINE BY USING DEXMEDETOMIDINE (A LOCAL ANAESTHETIC ADJUVANT) DURING SHOULDER ARTHROSCOPIC SURGERY

POST OPERATIVE OPIOID SPARING EFFECT OF INTRAVENOUS DEXMEDETOMIDINE IN PATIENTS UNDERGOING SHOULDER ARTHROSCOPY UNDER GENERAL ANAESTHESIA WITH ULTRASOUND GUIDED LOW DOSE INTERSCALENE BLOCK: A DOUBLE BLIND RANDOMIZED CONTROLLED STUDY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/049874
Enrollment
70
Registered
2023-02-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: S434- Sprain of shoulder joint

Interventions

Intervention1: Intravenous Dexmedetomidine : Intra operative Intravenous Dexmedetomidine is given at the dosage of 1 mcg/kg over 20 minutes in patients of shoulder arthroscopic surgery with low dose

Sponsors

BLK MAX SUPER SPECIALITY HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age group 18-50 years 2. ASA Grade I and II

Exclusion criteria

Exclusion criteria: 1. BMI >38 kg/m2 2. Pregnancy 3. Failure to provide written informed consent 4. Significant Psychiatric or Cognitive conditions interfering with consent or assessment 5. Pre-existing neurological deficits or neuropathy affecting the brachial plexus 6. Pre-existing chronic pain or opioid use 7. Significant renal or hepatic impairment 8. Severe bronchopulmonary disease including COPD and OSA 9. Contraindications to peripheral nerve block, including local skin infection, bleeding diathesis, coagulopathy, prior surgery in neck 10. Allergies to local anaesthetics, dexmedetomidine, or any component of multimodal analgesia

Design outcomes

Primary

MeasureTime frame
1. To study and compare the time required for the first rescue analgesia in the two groups. 2. To compare the total opioid consumption in the first 24 hours postoperatively between the two groups. Timepoint: 24 hours post operatively

Secondary

MeasureTime frame
1. To compare the patient satisfaction score between the two groups at the conclusion of first 24 hours. 2. To study and compare the adverse effects, if any, in the two groups.Timepoint: 24 hours post operatively

Countries

India

Contacts

Public ContactSUDDAPALLI SHAIK MOHAMMAD MALIK

BLK MAX SUPER SPECIALITY HOSPITAL

mvar1977@rediffmail.com

Outcome results

None listed

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