A Study Comparing Clove Spray and Lignocaine Spray to Reduce Throat Discomfort During Upper GI Endoscopy

Comparative Evaluation of Clove Spray and 10 Percent Lignocaine Spray as Topical Anesthetic for Oropharyngeal Anesthesia in upper GI Endoscopic Procedures: A Randomized Controlled Clinical Trial - nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/02/104455

Enrollment

Registered

2026-02-20

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

Health Condition 1: K30- Functional dyspepsia

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients aged 18 to 70 years. 2.Scheduled for diagnostic upper GI Endoscopy. 3.Patient with Complain of Dysphagia.

Exclusion criteria

Exclusion criteria: 1.Known hypersensitivity or allergy to clove or Lignocaine. 2.Presence of acute Throat infection, oral ulcers, or mucosal lesions. 3.Patients with Respiratory compromise, such as Asthma or COPD. 4.Patients with psychiatric disorders or neurological impairment that could affect reporting of symptoms or cooperation. 5.Any obstructive pathology in oral cavity

Design outcomes

Primary

Measure	Time frame
To observe onset and duration of Anesthesia following application of the herbal spray.Timepoint: Baseline, Day 0(immediately after intervention) Day 1 Day 2	—

Secondary

Measure	Time frame
To observe the unpleasant taste & nausea following application of the herbal spray.Timepoint: Baseline, Day 0(immediately after intervention) Day 1 Day 2	—

Countries

India

Contacts

Public ContactDr Mahesh P Jadhav

Dr D Y Patil college of Ayurveda and Research Centre Pimpri Pune

mahesh.jadhav@dpu.edu.in9096623998

Outcome results