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Optimal Balloon Catheter Placement During Sonohysterography

Primary Purpose

Infertility

Status
Completed
Phase
Phase 4
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
sonohysterography with inflated catheter in uterine cavity
sonohysterography with inflated catheter in cervical cavity
Sponsored by
Royan Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility focused on measuring Sonohysterography, catheter placement, pain magnitude, vasovagal reaction

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Infertile patients who will be referred to Royan institute for sonohysterography to evaluate the internal structure of uterine cavity (acquired & congenital abnormalities) are included in this prospective comparative study.

Exclusion Criteria:

  • Exclusion Criteria:

    • Symptoms of active pelvic infection
    • Abnormal uterine bleeding
    • Women with cervical stenosis
    • Women with each lesions which disrupts catheterization such as large myoma

Sites / Locations

  • Royan Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

patients with intrauterine balloon catheter placement

patients with intracervical balloon catheter placement

Arm Description

In this group, during the procedure of sonohysterography balloon catheter is inflated in the uterine cavity

During the procedure of sonohysterography balloon catheter is inflated in the cervical canal

Outcomes

Primary Outcome Measures

perceived Pain
inflation of the balloon & deflation of the balloon by a 10-point visual analog pain scale
Vasovagal reactions
Evaluation the vasovagal reactions (Hypotension, vomiting, syncope)in patients During procedure .
vasovagal reaction
Evaluation the vasovagal reactions (Hypotension, vomiting, syncope)in patients 30 minutes after procedure .

Secondary Outcome Measures

Saline volume
Evaluation the saline volume that is required for sonohisterography
time of procedure
Evaluation the total time that is needed for sonohysterography.

Full Information

First Posted
August 25, 2013
Last Updated
May 4, 2014
Sponsor
Royan Institute
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1. Study Identification

Unique Protocol Identification Number
NCT01936116
Brief Title
Optimal Balloon Catheter Placement During Sonohysterography
Official Title
Pain Perception and Side Effects During Sonohysterography With Balloon Catheters: a Randomized Comparative Study of Cervical With Uterine Catheter Placement
Study Type
Interventional

2. Study Status

Record Verification Date
February 2012
Overall Recruitment Status
Completed
Study Start Date
May 2012 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
October 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Royan Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Saline infusion sonohysterography and other intrauterine investigations methods may cause uterine cramping, pain and vasovagal reactions. According to few of previous studies the position of catheter placement can affect the magnitude of pain and amount of saline required during the sonohysterography. The purpose of this double blind control trial study is to assess whether the location of the balloon catheter either the uterus or cervix during sonohysterography can affect the magnitude of pain and the rate of vasovagal reaction.
Detailed Description
The proposal of study approved by the investigators institutional review boards and institution's ethical committee, and all participants will sign a written consent before enter to study. A total of 300 infertile women undergoing sonohysterography will be randomized to intrauterine or intracervical balloon catheter placement. The examination is scheduled in the early follicular phase of menstrual cycle, immediately after cessation of menstrual flow and before day 10. After preparation of patient, a 2 lumen 6-French flexible catheter is introduced into the cervical canal and balloon at the catheter tip is placed in the lower uterine segment or 1 cm into cervical canal and inflated with 1 mL of sterile saline solution. Under sonographic guidance, sterile normal saline solution (10-50 mL) is slowly introduced into the cavity until an adequate distention of the uterine cavity is obtained. Three-dimensional ultrasound scanned volumes are recorded. Patients are asked to assess their level of pain at the time of the balloon inflation and deflation using a 10-point visual analog pain scale. Patients are checked for the sign and symptoms of vasovagal reaction during and 30 minutes after procedure. Outcome measures will be assessed based on the intent-to-treat principle.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
Sonohysterography, catheter placement, pain magnitude, vasovagal reaction

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
300 (Actual)

8. Arms, Groups, and Interventions

Arm Title
patients with intrauterine balloon catheter placement
Arm Type
Experimental
Arm Description
In this group, during the procedure of sonohysterography balloon catheter is inflated in the uterine cavity
Arm Title
patients with intracervical balloon catheter placement
Arm Type
Active Comparator
Arm Description
During the procedure of sonohysterography balloon catheter is inflated in the cervical canal
Intervention Type
Device
Intervention Name(s)
sonohysterography with inflated catheter in uterine cavity
Intervention Description
during the procedure of sonohysterography balloon catheter is inflated in the uterine cavity
Intervention Type
Device
Intervention Name(s)
sonohysterography with inflated catheter in cervical cavity
Intervention Description
During the procedure of sonohysterography balloon catheter is inflated in the cervical canal
Primary Outcome Measure Information:
Title
perceived Pain
Description
inflation of the balloon & deflation of the balloon by a 10-point visual analog pain scale
Time Frame
during sonohysterography
Title
Vasovagal reactions
Description
Evaluation the vasovagal reactions (Hypotension, vomiting, syncope)in patients During procedure .
Time Frame
During sonohysterography
Title
vasovagal reaction
Description
Evaluation the vasovagal reactions (Hypotension, vomiting, syncope)in patients 30 minutes after procedure .
Time Frame
30 minutes after sonohysterography
Secondary Outcome Measure Information:
Title
Saline volume
Description
Evaluation the saline volume that is required for sonohisterography
Time Frame
during sonohysterography
Title
time of procedure
Description
Evaluation the total time that is needed for sonohysterography.
Time Frame
during sonohysterography

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infertile patients who will be referred to Royan institute for sonohysterography to evaluate the internal structure of uterine cavity (acquired & congenital abnormalities) are included in this prospective comparative study. Exclusion Criteria: Exclusion Criteria: Symptoms of active pelvic infection Abnormal uterine bleeding Women with cervical stenosis Women with each lesions which disrupts catheterization such as large myoma
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hamid Gourabi, PhD
Organizational Affiliation
Head of Royan Institute
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Fatemeh Zafarani, MSc
Organizational Affiliation
Department of Reproductive Imaging at Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Firoozeh Ahmadi, MD
Organizational Affiliation
Department of Reproductive Imaging at Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royan Institute
City
Tehran
Country
Iran, Islamic Republic of

12. IPD Sharing Statement

Links:
URL
http://royaninstitute.org
Description
Related Info

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Optimal Balloon Catheter Placement During Sonohysterography

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