Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT07124650

Sore Throat After Open Neck Elective Surgery

Led by Saint Petersburg State University, Russia · Updated on 2026-04-13

764

Participants Needed

1

Research Sites

84 weeks

Total Duration

On this page

Sponsors

S

Saint Petersburg State University, Russia

Lead Sponsor

S

Smooth Drug Development

Collaborating Sponsor

AI-Summary

What this Trial Is About

This randomized clinical trial aims to evaluate the effectiveness of two medications-hydrocortisone ointment and lidocaine solution-applied to the endotracheal tube in reducing postoperative throat pain, hoarseness, and cough following thyroid or parathyroid surgery with neuromonitoring. A total of 764 adult patients undergoing elective neck surgery at Saint-Petersburg State University Hospital will be enrolled and randomly assigned to receive either a hydrocortisone-coated or lidocaine-coated endotracheal tube. Outcomes will be assessed upon awakening from anesthesia, at 24 hours, and again at 3 days postoperatively. The findings may contribute to improving postoperative comfort and recovery for patients undergoing similar surgical procedures.

CONDITIONS

Official Title

Sore Throat After Open Neck Elective Surgery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients scheduled for elective open surgery on the thyroid/parathyroid glands with intraoperative neuromonitoring.
  • Age ≥18 years.
  • Willing and able to provide voluntary informed consent for participation in the study.
Not Eligible

You will not qualify if you...

  • Pregnancy (for women of childbearing potential).
  • Known allergy to hydrocortisone or lidocaine.
  • Refusal to participate in the study.

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Trial Site Locations

Total: 1 location

1

Saint Petersburg State University Hospital

Saint Petersburg, Russia

Actively Recruiting

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Research Team

S

Sergey M. Efremov, D. Med. Sc.

CONTACT

A

Alexey Y. Kulikov, Ph. D. (Med.)

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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