NCT06757920

Completed

"Bronchoscopic Argon Plasma Coagulation for Managing Endobro...

Alexandria University Source

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Other study identifiers

Sponsor study identifier

FOB - Endobronchial Carcinoid

Study Type

interventional

Actual enrollment (reported)

40

Locations

1 country

Sites

1

Timeline

Study Start

January 1, 2025

Actual (reported)

Primary Completion

July 15, 2025

Actual (reported)

Study Completion

August 20, 2025

Actual (reported)

Brief Summary

A small tube will go through the respiratory tract and a non contact cauterization will be done to the inside tumor

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 40 participants
Study completion date: August 20, 2025
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

First Submitted
December 27, 2024
Actual (reported)
Study Start
January 1, 2025
Actual (reported)
First Posted
January 3, 2025
Actual (reported)
Primary Completion
July 15, 2025
Actual (reported)
Study Completion
August 20, 2025
Actual (reported)

Last Updated: August 28, 2025
Status Verified: August 2025
Last Update Submitted: August 22, 2025

Conditions

Endobronchial Carcinoid

Keywords

Argon Plasma Coagulationfiberoptic bronchoscopyendobronchial carcinoid

Outcome Measures

Primary Outcomes (1)

Dyspnea Borg Scale
scale from 0 to 4 according to the degree of improvement
one month

Study Arms (1)

fiberoptic bronchoscopy in one group

ACTIVE COMPARATOR

fiberoptic bronchoscopic argon plasma coagulation for palliation of endobronchial carc inoid

Procedure: bronchoscopic argon plasma coagulation

Interventions

bronchoscopic argon plasma coagulationProcedure

Argon Plasma Cogulation for Debulking Endobronchial Carcinoid Using Fiberoptic Bronchoscopy

fiberoptic bronchoscopy in one group

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

Cooperative patient with written informed consent. 2- Patients diagnosed with endobronchial carcinoid. 3- Patients fit for fiberoptic bronchoscopy. 4- Patients unwilling or unfit for surgery.

You may not qualify if:

Sponsors & Collaborators

Alexandria University
Otherlead

Study Sites (1)

Chest Department -Faculty of Medicine

Alexandria, Azarita, 11511, Egypt

Study Officials

mohamed sabry eltarhony, lecturer
Alexandria University
PRINCIPAL INVESTIGATOR

Enrollment

40 participants (actual enrollment reported by the registry).

Study Design

Study Type: interventional
Phase: not applicable
Allocation: NA
Masking: NONE
Purpose: TREATMENT
Intervention Model: SINGLE GROUP
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Lecturer of chest diseases

Study Record Dates

First Submitted

December 27, 2024

First Posted

January 3, 2025

Study Start

January 1, 2025

Poor karnofsky score. 2- Patients unwilling or unfit for bronchoscopy. 3- Extraluminal lesion. 4- Patients with pacemaker. 5- Forced expiratory volume 1 is less than one litre.

Contact the study team to confirm eligibility.

Actual (reported)

Primary Completion

July 15, 2025

Actual (reported)

Study Completion

August 20, 2025

Actual (reported)

Last Updated

August 28, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing: Will not share

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT06757920
Data provider: ClinicalTrials.gov
Source updated: 2025-08-28
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:30:55 UTC

Locations

EG(1)

"Bronchoscopic Argon Plasma Coagulation for Managing Endobronchial Carcinoid Lesions

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

First Submitted

Study Start

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Study Arms (1)

fiberoptic bronchoscopy in one group

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

Related Links

Study Officials

Enrollment

Study Design

Study Record Dates

Data Sharing

Available IPD Datasets

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

Study Start

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Study Arms (1)

fiberoptic bronchoscopy in one group

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

Related Links

Study Officials

Enrollment

Study Design

Study Record Dates

Data Sharing

Available IPD Datasets

Source record

Locations