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LLETZ With Videocolposcopy Versus LLETZ With Binocular Colposcopy

Primary Purpose

Uterine Cervical Dysplasia

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
LLETZ with videocolposcope
LLETZ with binocular colposcope
Sponsored by
Zydolab - Institute of Cytology and Immune Cytochemistry
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Uterine Cervical Dysplasia focused on measuring conization, LLETZ, randomized controlled trial, colposcopy, binocular colposcopy, intraoperative colposcopy, videocolposcopy, loop excision

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • histologically proven cervical dysplasia
  • colposcopy Prior to conization
  • informed consent

Exclusion Criteria:

  • significant language barrier
  • a personal history of conization
  • pregnancy
  • the use of blood thinner
  • unwillingness to participate

Sites / Locations

  • Department of Obstetrics and Gynecology of the Ruhr University Bochum

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

LLETZ with videocolposcopy

LLETZ with binocular colposcopy

Arm Description

The LLETZ procedure will be performed using a videocolposcopy

The LLETZ procedure will be performed using a binocular colposcope

Outcomes

Primary Outcome Measures

the resected cone mass
the resected cone mass will be quantified by weighing the removed tissue with a precision scale located in the operating room

Secondary Outcome Measures

Margin status
Resection margin is judge as "R0" if abnormal cells are not found in the margin of the biopsy or "R1" if abnormal cells remain in the margin of the biopsy. The histopathological examination will be done by an Independent pathologist
Operation time
the time from the beginning of the Operation (start of the electrosurgical method) until the end of the operation (the end of hemostatic interventions) will be measured in minutes
Operative complications
Operative complications defined as necessity to intervene therapeutically up to 14 days postoperatively
number of fragments of the surgical specimen
surgeons will count the number of the surgical specimen (1 vs. >1)
The circumference of the surgical specimens
The circumference of the surgical specimens will be measured in cm
the length of the surgical specimens
The length of The surgical specimens will be measured in cm
the thickness of the surgical specimens
The thickness of The surgical specimens will be measured in cm
handling of the device
surgeons will score their preference regarding the surgical method using an 11-step visual analogue scale (VAS) for ,(ranging from 0 (,very easy') to 10 (,very difficult')
satisfaction with the device
surgeons will score their preference regarding the surgical method using an 11-step visual analogue scale (VAS) for ,satisfaction with the device' (ranging from 0 (,very satisfied') to 10 (,absolutely not satisfied')
Time to complete intraoperative hemostasis
the time until complete hemostasis as judged by the surgeon has been achieved, will be measured in seconds
Intraoperative blood loss
intraoperative blood loss will be measured using the difference in serum hemoglobin one day prior to surgery and within 5 hours postoperatively

Full Information

First Posted
March 25, 2020
Last Updated
July 17, 2022
Sponsor
Zydolab - Institute of Cytology and Immune Cytochemistry
Collaborators
Ruhr University of Bochum
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1. Study Identification

Unique Protocol Identification Number
NCT04326049
Brief Title
LLETZ With Videocolposcopy Versus LLETZ With Binocular Colposcopy
Official Title
Performance of Large Loop Excision of the Transformation Zone Using Videocolposcopy Versus Binocular Colposcopy in Women With Cervical Dysplasia: a Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
March 25, 2020 (Actual)
Primary Completion Date
March 28, 2021 (Actual)
Study Completion Date
June 29, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zydolab - Institute of Cytology and Immune Cytochemistry
Collaborators
Ruhr University of Bochum

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
To assess the benefits of performing large Loop excision of the transformation Zone (LLETZ) using videocolposcopy compared to binocular colposcopy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Uterine Cervical Dysplasia
Keywords
conization, LLETZ, randomized controlled trial, colposcopy, binocular colposcopy, intraoperative colposcopy, videocolposcopy, loop excision

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
227 (Actual)

8. Arms, Groups, and Interventions

Arm Title
LLETZ with videocolposcopy
Arm Type
Experimental
Arm Description
The LLETZ procedure will be performed using a videocolposcopy
Arm Title
LLETZ with binocular colposcopy
Arm Type
Active Comparator
Arm Description
The LLETZ procedure will be performed using a binocular colposcope
Intervention Type
Device
Intervention Name(s)
LLETZ with videocolposcope
Intervention Description
Loop procedure using a videocolposcope in order to see and remove the abnormal cervical tissue
Intervention Type
Device
Intervention Name(s)
LLETZ with binocular colposcope
Intervention Description
Loop procedure using a binocular colposcope in order to see and remove the abnormal cervical tissue
Primary Outcome Measure Information:
Title
the resected cone mass
Description
the resected cone mass will be quantified by weighing the removed tissue with a precision scale located in the operating room
Time Frame
10 minutes
Secondary Outcome Measure Information:
Title
Margin status
Description
Resection margin is judge as "R0" if abnormal cells are not found in the margin of the biopsy or "R1" if abnormal cells remain in the margin of the biopsy. The histopathological examination will be done by an Independent pathologist
Time Frame
2 Days after conization
Title
Operation time
Description
the time from the beginning of the Operation (start of the electrosurgical method) until the end of the operation (the end of hemostatic interventions) will be measured in minutes
Time Frame
20 minutes
Title
Operative complications
Description
Operative complications defined as necessity to intervene therapeutically up to 14 days postoperatively
Time Frame
14 days
Title
number of fragments of the surgical specimen
Description
surgeons will count the number of the surgical specimen (1 vs. >1)
Time Frame
10 minutes
Title
The circumference of the surgical specimens
Description
The circumference of the surgical specimens will be measured in cm
Time Frame
2 Days after conization
Title
the length of the surgical specimens
Description
The length of The surgical specimens will be measured in cm
Time Frame
2 Days after conization
Title
the thickness of the surgical specimens
Description
The thickness of The surgical specimens will be measured in cm
Time Frame
2 Days after conization
Title
handling of the device
Description
surgeons will score their preference regarding the surgical method using an 11-step visual analogue scale (VAS) for ,(ranging from 0 (,very easy') to 10 (,very difficult')
Time Frame
30 minutes
Title
satisfaction with the device
Description
surgeons will score their preference regarding the surgical method using an 11-step visual analogue scale (VAS) for ,satisfaction with the device' (ranging from 0 (,very satisfied') to 10 (,absolutely not satisfied')
Time Frame
30 minutes
Title
Time to complete intraoperative hemostasis
Description
the time until complete hemostasis as judged by the surgeon has been achieved, will be measured in seconds
Time Frame
120 seconds
Title
Intraoperative blood loss
Description
intraoperative blood loss will be measured using the difference in serum hemoglobin one day prior to surgery and within 5 hours postoperatively
Time Frame
5 hours

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: histologically proven cervical dysplasia colposcopy Prior to conization informed consent Exclusion Criteria: significant language barrier a personal history of conization pregnancy the use of blood thinner unwillingness to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ziad Hilal, M.D.
Organizational Affiliation
Zydolab - Institute of Cytology and Immune Cytochemistry
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Obstetrics and Gynecology of the Ruhr University Bochum
City
Herne
State/Province
NRW
ZIP/Postal Code
44625
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34802113
Citation
Rezniczek GA, Neghabian N, Rehman S, Tempfer CB. Video colposcopy versus headlight for large loop excision of the transformation zone (LLETZ): a randomised trial. Arch Gynecol Obstet. 2022 Feb;305(2):415-423. doi: 10.1007/s00404-021-06331-0. Epub 2021 Nov 21.
Results Reference
derived

Learn more about this trial

LLETZ With Videocolposcopy Versus LLETZ With Binocular Colposcopy

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