MedPath

To compare audiovisual technology as distraction technique with sedatives for treating anxiety for upperlimb surgeries

Phase 4
Conditions
Health Condition 1: M80-M85- Disorders of bone density and structureHealth Condition 2: M65-M67- Disorders of synovium and tendonHealth Condition 3: M70-M79- Other soft tissue disorders
Registration Number
CTRI/2024/03/064672
Lead Sponsor
Dr KUMARA
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients who give consent

Exclusion Criteria

Significant Psychiatric disorder such as Generalized Anxiety disorder, Panic disorder, Depression, Psychosis, Bipolar disorder,

Pregnant and or Breastfeeding Patient,

Underlying Coagulopathies,

Infections at the site,

Hypersensitivity to sedatives

History of renal impairment.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate anxiety rating between two groups receiving two different interventions, namely audio visual distraction and sedatives in decreasing anxiety post brachial plexus block administration.Timepoint: 0 minute (post operative)
Secondary Outcome Measures
NameTimeMethod
comparing hemodynamic parameters in both the groups.Timepoint: 5minutes, 10minutes, 15minutes, 30minutes, 1hour, 1hour 30minutes.(intra operative)
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