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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03311893
Other study ID # 2016/199
Secondary ID
Status Completed
Phase N/A
First received September 13, 2017
Last updated October 11, 2017
Start date October 10, 2016
Est. completion date August 10, 2017

Study information

Verified date October 2016
Source Inonu University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

200 participants' perception and acceptability of natural hole surgeon


Description:

100 participants health personnel 100 participants population two group's perception and acceptability of natural orifice surgeon


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date August 10, 2017
Est. primary completion date July 10, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 17 Years to 100 Years
Eligibility Inclusion Criteria:

- all female (health personnel and population)

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
natural orifice surgery
evaluation of the awareness of the use of transvaginal, transoral and transcranial approach in surgical excision and the difference between the health staff and the pathology

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Inonu University

Outcome

Type Measure Description Time frame Safety issue
Primary natural orifice surgery a survey study that measures the awareness of natural orifice surgery 12 months
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