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A clinical trial to study the effect of addition of oral zinc or placebo with local anesthetic lignocaine over vocal cords in reducing the postoperative sore throat after general anesthesia.

The effect of addition of oral zinc or placebo to lignocaine instillation in reducing the postoperative sore throat after general endotracheal anesthesia: A prospective randomized double blind study. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/063725
Enrollment
120
Registered
2024-03-06
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: - Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: lignocaine solution: lignocaine 80 mg over glottis during intubation Control Intervention1: oral zinc and lignocaine solution: oral zinc 40 mg 30 minutes prior to intubation and lignoc

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients aged 18 to 65 years. 2.Patients with American Society of Anesthesiologists (ASA) physical status [19] I to II. 3.Patients with Mallampatti grade (MPG) I & II 4.Patients scheduled to undergo elective surgery of 4 hours duration who requires general endotracheal anaesthesia.

Exclusion criteria

Exclusion criteria: 1.Patients with pre-existing steroid or non-steroidal anti-inflammatory drug use. 2.Patients who will be on Zinc supplements. 3.Patients having history of preoperative sore throat or recent upper airway infection, asthma, chronic obstructive pulmonary disease. 4.Patients with known or anticipated difficult airway. 5.Patients with known allergy to study drug. 6.Known smoker. 7.Pregnant and lactating women. 8.Patients not willing to give consent

Design outcomes

Primary

MeasureTime frame
occurrence of postoperative sore throat after tracheal extubationTimepoint: At 0 min , 1st hour , 2nd hour , 4th hour , 6 th hour and 24hrs

Secondary

MeasureTime frame
1.Severity of postoperative sore throat. 2.Severity of post-operative cough 3.The severity postoperative hoarseness Timepoint: at 0, 1, 2, 4, 6 and 24 hours after tracheal extubation

Countries

India

Contacts

Public ContactDr M Madhusudan

Sri Venkateswara Institute of Medical Sciences

drmadhu37@gmail.com9493547723

Outcome results

None listed

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