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

ConditionThroat, Sore
Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18-60
SponsorUniversity of Malaya

About this trial

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.

Eligibility criteria

Qualifiers

Classified as ASA I-II, indicating a relatively low risk of complications from anesthesia

Aged between 18 and 60 years, which represents a typical adult surgical population

Both male and female patients, ensuring gender inclusivity and representation in the study findings

Disqualifiers

Existing sore throat prior to surgery, which could affect the baseline measurement of postoperative sore throat.

Anticipation of a difficult airway, as these patients may require specialized intubation techniques that are not standardized across the study.

More than two attempts at endotracheal tube (ETT) insertion, as multiple attempts could cause additional trauma and skew the study outcomes.

Any trauma occurring during intubation, which could independently contribute to postoperative sore throat and other complications

Trial design

Treatments tested in this trial

  • Gengigel

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators