Skip to main content
OpenTrials
Completed

NCT Number: NCT05036525

Evaluation of the Efficacy and Safety of a Hyaluronic Acid Gel in Adhesion Prevention After Open Thyroidectomy.

The aim of this study is to assess the safety and efficacy of HANBIO BarriGel to prevent thyroidectomy postoperative adhesions

Completed

Looking for future studies?

Notify Me

Key information

Age range

20 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kaohsiung Chang Gung Memorial Hospital, Kaohsiung City, Taiwan

Loading trial locations.

About this study

The objective of this study is to evaluate the efficacy of HANBIO BarriGel in the prevention of postoperative adhesion for patients who will undergo open thyroidectomy. The dysphagia and adhesion severity will be assessed at specific visits pre and/or post-operation for both treatment group and control group. The post-operative condition, and the adverse event information will be collected for evaluation of tolerability and safety of the product.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female between 20 and 70 years of age.
  • Patients diagnosed with benign goiter or thyroid cancer that will undergo open thyroidectomy (either unilateral or bilateral total thyroidectomy with or without central lymph node dissection).
  • Naïve patients to thyroid surgery.
  • Subjects are willing to comply with all aspects of the study and have signed informed consent form.

Exclusion criteria

  • Pregnant or lactating female patients.
  • Presence of severe and uncontrolled illness such as stroke, hypertension, diabetes, chronic renal failure, coagulopathy, drug abuse.
  • Patients with previous neck radiotherapy within 1 year.
  • Concurrent diseases/conditions which will be unable to evaluate the outcomes.
  • Patients receiving any adhesion prevention adjuvant.
  • Previous history of Keloid or hypertrophic scar.
  • Anticoagulant used within a week from surgery.
  • Subjects are hypersensitive to sodium hyaluronate.
  • Participate in another clinical trial within 1 month.
  • Patients presence of surgical site infection.
  • Patients are with abnormal clinical test (appendix 1) result within one month or ECOG performance status (appendix 2) score ranged from 3-4.

Treatment and study plan

HANBIO BarriGel

Device

an anti-adhesive product

Primary outcomes

  1. Dysphagia Handicap Index (DHI)

    Time frame: Preoperative 6 weeks

Sponsors and collaborators

Lead sponsor

HAN Biomedical Inc

Industry

Registry information

Official study title

Evaluation of the Efficacy and Safety of a High Molecular Weight Native Hyaluronic Acid Gel (HANBIO BarriGel) in Adhesion Prevention After Open Thyroidectomy: a Prospective, Randomized Controlled, Single Blind Study.

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Sep 5, 2021
Registry last updated
Mar 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.