Actively Recruiting

Early Phase 1
Age: 18Years - 60Years
All Genders
Healthy Volunteers
NCT06947161

Pilot Study of Throat Packs Soaked in Gengigel Spray in Patients Undergoing Elective Surgery

Led by University of Malaya · Updated on 2025-04-27

60

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Throat packs are commonly used in many surgical procedures involving the oral cavity and pharynx, primarily to prevent blood, saliva, and other debris from entering the lower respiratory tract, thereby maintaining a clear airway and reducing the risk of aspiration and respiratory complications. Traditionally, these packs are moistened with saline or used in a dry state, with the choice often depending on the surgeon's preference and specific surgical requirements. However, despite their widespread usage, the exploration of alternative substances to moisten throat packs, particularly those with additional therapeutic benefits, remains limited in medical research. This pilot study introduces Gengigel spray as an innovative alternative to saline for moistening throat packs. Gengigel, a hyaluronic acid (HA)-based product, is known for its healing properties and anti-inflammatory effects, which are beneficial in oral care. Gengigel provides a non-anesthetic approach that promotes tissue repair and reduces inflammation. This makes it particularly advantageous in the context of surgical procedures where reducing postoperative inflammation and promoting mucosal healing are crucial.

CONDITIONS

Official Title

Pilot Study of Throat Packs Soaked in Gengigel Spray in Patients Undergoing Elective Surgery

Who Can Participate

Age: 18Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Classified as ASA I-II, indicating low risk for anesthesia complications
  • Aged between 18 and 60 years
  • Male and female patients included
Not Eligible

You will not qualify if you...

  • Existing sore throat before surgery
  • Anticipated difficult airway
  • More than two attempts at endotracheal tube insertion
  • Trauma occurring during intubation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sabreena Ismail

Kuala Lumpur, Malaysia, 50603

Actively Recruiting

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Research Team

S

sabreena ismail, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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