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Clinical Study of Curcumin in Preventing Postoperative Adhesion of Bilateral Vocal Cords

E

Eye & ENT Hospital of Fudan University

Status and phase

Enrolling
Phase 2
Phase 1

Conditions

Laryngeal Leucoplakia
Laryngeal Polyp
Laryngeal Papilloma
Glottic Carcinoma
Glottic Web of Larynx
Laryngeal Stenosis

Treatments

Drug: Curcumin
Drug: Mitomycin-C

Study type

Interventional

Funder types

Other

Identifiers

NCT05688488
2022011-1

Details and patient eligibility

About

To provide a novel therapy idea and method to solve the clinical problem of postoperative adhesion of bilateral vocal cords, patients enrolled in this study will be applied with curcumin on both wound sites of bilateral vocal cords after the surgery on the bilateral vocal cord endoscopically.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients with bilateral vocal cord diseases who are going to undergo resection of bilateral vocal cord lesions endoscopically.
  2. Patients with bilateral vocal cord adhesion who are going to undergo incision of bilateral vocal cord adhesion endoscopically.

Exclusion criteria

  1. Patients with other laryngeal diseases.
  2. Patients with cardiac and pulmonary insufficiency.
  3. Patients unable to cooperate with the follow-up on time after surgery.
  4. Patients who refuse to sign the informed consent after notification.
  5. Patients who have a severe allergic disease or allergic history to a variety of drugs.
  6. Other circumstances that are not appropriate to be included in the clinical trial.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

100 participants in 2 patient groups

Curcumin
Experimental group
Treatment:
Drug: Curcumin
Mitomycin
Active Comparator group
Treatment:
Drug: Mitomycin-C

Trial contacts and locations

1

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Central trial contact

Haitao Wu, Ph.D; Jian Chen, Ph.D

Data sourced from clinicaltrials.gov

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