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A study comparing duration of postoperative analgesia after shoulder block in patients undergoing shoulder arthroscopy.

comparative evaluation of effect of intravenous dexmedetomidine on duration of postoperative analgesia after shoulder block in patients undergoing shoulder arthroscopy.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/11/029253
Enrollment
50
Registered
2020-11-19
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: M258- Other specified joint disorders

Interventions

Intervention1: Shoulder block with 10 ml of 0.5% ropivacaine with 1:200000 ADR each in suprascapular and axillary nerve block before GA induction followed by 0.5mcg/kg intravenous dexmedetomidine dilu

Sponsors

Vardhman Mahavir Medical College and Safdarjung hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1-2, scheduled for elective unilateral arthroscopic shoulder surgery.

Exclusion criteria

Exclusion criteria: 1) history of allergy to local anaesthetic 2) contraindication to block 3) previous neurological deficit in upper limb 4) BMI >30 KG/m2 5) inability to understand pain scale (VAS) 6) pulmonary, renal, cardiac, hepatic disease

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy and duration of post-op analgesia provided by intravenous dexmedetomidine after shoulder block using VAS.Timepoint: 0,2,4,6,12,24 hours—

Secondary

MeasureTime frame
To compare patient satisfaction in form of quality of pain relief using LIKERT SCALETimepoint: 24 hrs;To compare total amount of rescue analgesia required in each group over 24 hours.Timepoint: 0,2,4,6,12,24—

Countries

India

Contacts

Public ContactDr Suman Saini

Vardhman Mahavir Medical College and Safdarjung hospital

drsainisumannony@gmail.com9891228793

Outcome results

None listed

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