NCT03311893

Brief Summary

200 participants' perception and acceptability of natural hole surgeon

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
200

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2016

Shorter than P25 for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 10, 2016

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 10, 2017

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 10, 2017

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

September 13, 2017

Completed
1 month until next milestone

First Posted

Study publicly available on registry

October 17, 2017

Completed
Last Updated

October 17, 2017

Status Verified

October 1, 2016

Enrollment Period

9 months

First QC Date

September 13, 2017

Last Update Submit

October 11, 2017

Conditions

Health, Subjective

Outcome Measures

Primary Outcomes (1)

  • natural orifice surgery

    a survey study that measures the awareness of natural orifice surgery

    12 months

Study Arms (2)

health personnel

ACTIVE COMPARATOR

natural orifice surgery evaluation of the awareness of the use of transvaginal, transoral and trananal approach in surgical excision and the difference between the health staff and population

Procedure: natural orifice surgery

population

PLACEBO COMPARATOR

natural orifice surgery evaluation of the awareness of the use of transvaginal, transoral and trananal approach in surgical excision and the difference between the health staff and population

Procedure: natural orifice surgery

Interventions

natural orifice surgeryPROCEDURE

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

health personnelpopulation

Eligibility Criteria

Age17 Years - 100 Years
Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • all female (health personnel and population)

You may not qualify if:

  • none

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Natural Orifice Endoscopic Surgery

Intervention Hierarchy (Ancestors)

EndoscopyDiagnostic Techniques, SurgicalDiagnostic Techniques and ProceduresDiagnosisMinimally Invasive Surgical ProceduresSurgical Procedures, Operative

Study Officials

  • Ersin Gündoğan, MD

    Inonu Unıversity- general surgery

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
operator doctor

Study Record Dates

First Submitted

September 13, 2017

First Posted

October 17, 2017

Study Start

October 10, 2016

Primary Completion

July 10, 2017

Study Completion

August 10, 2017

Last Updated

October 17, 2017

Record last verified: 2016-10