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Effect of Clove oil gargle on reducing postoperative sore throat following general anaesthesia.

Effect of clove oil gargle on the incidence and severity of postoperative sore throat following endotracheal intubation in adult patients undergoing surgery-a randomized placebo-controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/040907
Enrollment
134
Registered
2022-03-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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: Pre operative Clove oil gargle: Gargling with Clove oil diluted in 20 ml of tap water 15 mins prior to surgery Control Intervention1: Pre operative tap water gargle: Gargling with 20 ml

Sponsors

Dr Neingutso Lomi
Lead Sponsor
Dr Sritam Swarup Jena
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1)ASA Grade I & II patients undergoing elective surgery 2)Age- 18 to 65 years 3)Expected duration of surgery 4)Airway- Mallampati Grade 1 & 2

Exclusion criteria

Exclusion criteria: 1)Patients not willing to give consent 2)Patients with sore throat, cold, gastroesophageal reflux, regurgitation 3)Patients with anticipated difficult airway 4)Patients with oral/oro-pharyngeal/laryngeal pathology for which the current surgery is planned or airway surgeries 5)Patients on steroid therapy 6)Surgery lasting for > 3 hours 7)Patients requiring second laryngoscopy for nasogastric tube insertion or throat packing or unanticipated difficult airway 8)Patients who remain intubated/require re-intubation post surgery 9)Recent history of surgery under general anaesthesia/airway instrumentation 10)Patients in whom extubation provokes extreme degree of coughing/bucking on tube 11)Patients requiring flexometallic tubes 12)Patients in prone position

Design outcomes

Primary

MeasureTime frame
Incidence of sore throatTimepoint: Postoperatively at 6 hours

Secondary

MeasureTime frame
Adverse effectsTimepoint: Until 24 hr;Incidence of sore throatTimepoint: 0 hr, 30 mins, 1 hr, 2 hr, & 24 hr;Patient satisfaction with interventions for sore throatTimepoint: Postoperatively at 24 hr;Severity of sore throatTimepoint: 0 hr, 30 min, 1 hr, 2 hr, 6 hr, & 24 hr

Countries

India

Contacts

Public ContactDr Sritam Swarup Jena

AIIMS Bhubaneswar

anaes_sritam@aiimsbhubaneswar.edu.in8951614718

Outcome results

None listed

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