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Protocol for Anatomopathologic Analysis of Biopsies Using Hot Clamps

Protocol for Anatomopathologic Analysis of Biopsies Using Hot Clamps

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02887378
Acronym
PincesChaude
Enrollment
46
Registered
2016-09-02
Start date
2014-09-30
Completion date
2016-09-30
Last updated
2016-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endoscopy

Keywords

bronchial biopsy

Brief summary

A cross-over study of the impact of histologic results of bronchial biopsies performed using hot clamps compared to bronchial biopsies using standard clamps

Interventions

DEVICEhot clamps

reusable hot biopsy forceps

DEVICEnormal clamps

Sponsors

Centre Hospitalier Universitaire, Amiens
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients 18 years of age or older * Patients with no known hemorrhage risk, with an indication of endobronchial biopsy * Patients with no contra-indication for bronchial endoscopy * Patients with or without endobronchial tumors * Patients who have provided written informed consent * Patients with health insurance coverage

Exclusion criteria

* Refusal to be examined * Contraindication for electrocoagulation (Pacemaker or metallic endobronchial prosthesis) * Pregnant women * Patients unable to provide voluntary informed consent, under (tutelage) or guardianship, or unable to come to the center

Design outcomes

Primary

MeasureTime frameDescription
use of reusable hot biopsy forceps2 yearsTo show that the use of hot clamps (thermocoagulating) for endobronchial analysis does not affect the anatomopathologic interpretation of biopsies under certain conditions (with varying in intensity of current).

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026