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NCT Number: NCT06287034

The Role of the Free/Pedunculated Flap in Total Laryngectomy After (Chemo-)Radiotherapy Failure for Laryngeal Carcinoma: Impact on the Risk of Pharyngocutaneous Fistula (PCF)

Multicenter, prospective, randomized study aimed at evaluating the difference in risk of PCF after salvage laryngectomy in two groups of patients: one cohort treated with Total Laryngectomy (LT) with primary suture, a second group treated with LT and reinforcement by flap positioning with onlay technique (PMM, ALT)

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

"Regina Elena" National Cancer Institute

Rome, 00144, Italy

Location status: Recruiting

Location contact

Pellini Raul, Doctor

CONTACT

[email protected]

06-52664484

About this study

Patients, once eligibility has been verified, will then be randomized (1:1) to one of the following groups: Gruop 1: STL primary suture. Group 2: STL primary suture + onlay flap Patients in both groups will then undergo surgery STL with primary suture; in those of the second group, in addition, the positioning of a free/pedunculated covering flap will also be carried out with the onlay technique. 4 months after surgery, questionnaires will be administered to the patient for the subjective evaluation of the quality of life in relation to vocal rehabilitation obtained through voice prosthesis or esophageal voice (SECEL questionnaire) and swallowing rehabilitation (SOAL questionnaire). Demographic and preoperative data will be collected, data relating to pre-(chemo-)radiotherapy and pre-STL clinical staging, as well as the interval in days between the end of (chemo-)radiotherapy and surgery, perioperative data, type of eventual unilateral or bilateral laterocervical lymph node emptying, the type of pharyngotomy suture, the type of flap possibly used, the packaging of the tracheoesophageal fistula for positioning the voice prosthesis, the definitive histological examination.

The patient must undergo a radiological examination for loco-regional and distant staging before the STL (CT or MRI) and a biopsy demonstrating the recurrence/persistence of the disease.

Who can participate

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

Inclusion criteria

  • Histological confirmation of recurrence/persistence of squamous cell carcinoma of the larynx previously subjected to exclusive radiotherapy or concomitant chemo-radiotherapy treatment:
  • pre (ChT-)RT staging: cT1/T2/T3 N0/N+;
  • pre STL staging: rcT1/cT2/ Selected cT3 cT4a (extension to thyroid cartilage and/or prelaryngeal tissues) N0/N+ (clinically and radiologically).
  • Indication for STL surgery (no pharyngeal mucosal resection);
  • Functional total laryngectomies after radical (chemo-)radiotherapy treatment;
  • Age > 18 years;
  • Signature of informed consent and ability to complete in-office questionnaires.

Exclusion criteria

  • STL extended to the pharynx and/or total pharyngeal laryngectomies;
  • Extension of the tumor to the pharyngeal mucosa and/or massive extra-laryngeal extension;
  • Previous open organ preservation surgery (OPHL).

Treatment and study plan

Primary suture

Procedure

The primary suture can be performed according to the different techniques available at the discretion of the surgeon (vertical, horizontal or T-shaped closure, with continuous suture, according to Connell or with detached stitches)

Primary outcomes

  1. questionnaires for evaluation of the quality of life

    Time frame: 30 months

    Questionnaires will be administered to the patient for the subjective evaluation of the quality of life in relation to vocal rehabilitation obtained through voice prosthesis or esophageal voice (SECEL questionnaire).

Secondary outcomes

  1. Identification of risk factors

    Time frame: 4 months

    Identification of risk factors related to the formation of pharyngocutaneous fistulas after salvage total laryngectomy

  2. Evaluation of swallowing function

    Time frame: 4 months

    Evaluation of swallowing function assessed using the SOAL questionnaire

  3. Evaluation of vocal rehabilitation

    Time frame: 4 months

    Evaluation of vocal rehabilitation using the SECEL questionnaire

Study contacts

Contact information is provided by the study sponsor or research team.

Raul Pellini, Doctor

CONTACT

[email protected]

06-52664484 ext. +39

Sponsors and collaborators

Lead sponsor

Regina Elena Cancer Institute

Other

Registry information

Important dates

Study start
2023
Primary completion
2025
Study completion
2027
First posted
Feb 29, 2024
Registry last updated
Jun 5, 2026

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.

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