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A Randomized, Double-Blinded Comparative Study of Pre-Operative Nebulized Dexamethasone and Intravenous Ketorolac Tromethamine for the Prevention of Post-Operative Sore Throat Following General Anesthesia

A Randomized, Double-Blinded Comparative Study of Pre-Operative Nebulized Dexamethasone and Intravenous Ketorolac Tromethamine for the Prevention of Post-Operative Sore Throat Following General Anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260222068917N1
Enrollment
100
Registered
2026-02-25
Start date
2025-07-16
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Postoperative Sore Throat (POST) following General Anesthesia.

Interventions

Intervention 1: Intervention Group 1: Group D – Dexamethasone, Participants receive preoperative nebulized dexamethasone, 15–30 minutes before induction of general anesthesia. Intervention 2: Interven

Sponsors

Superior University, Lahore
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patients aged 18 – 50 undergoing surgeries that require endotracheal intubation after general anesthesia ASA Physical status of I–III Patient giving informed consent.

Exclusion criteria

Exclusion criteria: Patient known to be allergic to study drugs Asthmatic or COPD patients ASA physical status IV – VI The Patient has a pre-existing sore throat or pain Surgeries involving the neck, throat, or airway Upper respiratory tract infection Patients with a history of renal disease

Design outcomes

Primary

MeasureTime frame
Incidence and Severity of Postoperative Sore Throat (POST). Timepoint: Measured at 2, 4, 6, and 12 hours after extubation. Method of measurement: Severity was assessed using the STAT-10 scale, a validated questionnaire for postoperative sore throat.Incidence is recorded as the presence or absence of sore throat at each time point.

Secondary

MeasureTime frame
. Timepoint: . Method of measurement: .;Secondary outcomes include intubation-related factors (number of attempts and their association with POST severity), cuff pressure categories (=24 vs >24 cm H2O), surgery-related factors (type and duration of surgery), endotracheal tube size, postoperative complications (nausea, vomiting, GI irritation, hyperglycemia, delayed wound healing, and others), and requirement for rescue analgesia. Timepoint: Secondary outcomes was measured at 2, 4, 6, and 12 hours after extubation for outcomes related to POST and complications. Method of measurement: The secondary outcomes are measured using a combination of direct observation, structured questionnaires, and patient records. Intubation attempts and endotracheal tube size are recorded intraoperatively from anesthesia notes. Cuff pressure is measured using a manometer at the time of intubation. Surgery type and duration are documented from operative records. Postoperative complications such as nausea, vomiting, GI irritation, hyperglycemia, delayed wound healing, and others are monitored through direct observation and patient self-report. Rescue analgesia requirement is recorded from patient charts and by direct inquiry during the 12-hour postoperative period. Outcome assessors are blinded to group allocation to minimize bias.

Countries

Pakistan

Contacts

Public ContactAbdul Mabood

Superior University, Lahore

abdulmabood856@gmail.com+92 345 8561831

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026