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NCT05932537 Clinical Trial

Ablation of Subcutaneous Contraceptive Implants in the Operating Room

Contraceptive Usage Clinical Trial

— TAICS  

Official title:
Technical Description of the Ablation of Subcutaneous Contraceptive Implants in the Operating Room

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05932537
Other study ID # 69HCL22_1032
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 15, 2022
Est. completion date December 31, 2023

Study information
Verified date July 2023
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The ablation of subcutaneous contraceptive implants is usually performed in consultation under local anesthesia. However, it happens that the implant was placed too deeply or that it migrated too deeply making it impossible to remove it in consultation. These patients should then be referred to reference centers so that the explantation takes place in the operating room. The investigators propose to describe their techniques for preoperative visualization of the implant and their techniques for surgical explantation for educational purposes.

Recruitment information / eligibility
Status Recruiting
Enrollment 50
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - women over 18 - patient who underwent explantation of a subcutaneous contraceptive implant in the gynecology operating room - intervention between 2018 and 2022 - person having expressed his non-opposition Exclusion Criteria: - explantation outside the operating room - inability to understand the information given - person deprived of liberty - person under guardianship

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Preoperative visualization techniques
describe techniques for pre-operative visualization of subcutaneous contraceptive implants

Locations
Country Name City State
France Gynaecology Department, Hôpital Femme Mère Enfant, Hospices Civils de Lyon Bron

Sponsors (1)
Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Ultrasound for visualization of implants Percentage of patients with an ultrasound to visualize the implants preoperatively
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