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Video laryngoscopy and intravenous dexamethasone outcome on sore throat post surgery

Effect of intravenous dexamethasone, video laryngoscopy or their combination on post operative sore throat in adults undergoing surgery: A randomized double blinded placebo control trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073161
Enrollment
220
Registered
2024-09-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Interventions

Intervention1: Video laryngoscopy and intravenous dexamethasone: The patients will be randomized into 4 study groups and followed up for sore throat in 0th, 1st, 2nd, 6th and 24th hour post extubation

Sponsors

AIIMS Bhubaneswar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults aged 18 to 65 years of either gender ASA grade 1 and 2 Scheduled for elective surgery under general anaesthesia� requiring endotracheal intubation Duration more than 1 hour and less than 3 hours

Exclusion criteria

Exclusion criteria: Patient refusal Diabetes mellitus Known allergy or contraindication to use of corticosteroids�  More than 2 attempts at intubation or unanticipated difficult airway Pre operative assessment of difficult airway�  Pre operative sore throat, cough or recurrent respiratory infection� in last 2 weeks Surgeries which require nasogastric tube insertion or throat pack Patient undergoing any surgery of airway�  Patient undergoing surgery in prone position Need of post operative mechanical ventilation Risk of aspiration Pregnancy�  Pre operatively taking pain medications History of opioid abuse and smoking Prior anaesthetic exposure within one month

Design outcomes

Primary

MeasureTime frame
To evaluate incidence of postoperative sore throat at the 6th hour post extubation in patients undergoing surgery requiring general anaesthesia under endotracheal intubationTimepoint: 6th hour post extubation

Secondary

MeasureTime frame
To determine the incidence of POST at 0th, 1st, 2nd and 24th hour post extubation. To determine severity of POST at 0th, 1st, 2nd, 6th and 24th hour post extubation. To determine the incidence and severity of post operative cough and hoarseness of voice at 0th, 1st, 2nd, 6th, 24th hour post extubation To determine patient satisfaction at 6 hours, post extubationTimepoint: 0th,1st,2nd,24th hour post extubation

Countries

India

Contacts

Public ContactDr Maharshi Bhattacharyya

AIIMS Bhubaneswar

001maharshi001@gmail.com9113855768

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 27, 2026