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Ultrasound Device for Infertility (SELF-GYN1 Trial)

N/A

Waitlist Available

Research Sponsored by Turtle Health, Inc.

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up 1 year

Awards & highlights

SELF-GYN1 Trial Summary

This trial will test how well a layperson can follow instructions to use an at-home ultrasound machine to get accurate images, with the help of a remote technician.

SELF-GYN1 Trial Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 1 year

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~1 year

This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Image Quality

Net Promoter Score (NPS)

Secondary outcome measures

All Other Adverse Events

Box Opening

Correct Cavity

+15 more

SELF-GYN1 Trial Design

1Treatment groups

Experimental Treatment

Group I: Ultrasound DeviceExperimental Treatment1 Intervention

All women who choose to enroll in the trial will undergo an at home transvaginal ultrasound guided by real-time remote supervision from a qualified and specially trained ultrasound technologist.

Treatment

First Studied

Drug Approval Stage

How many patients have taken this drug

Transvaginal ultrasound

2013

Completed Phase 3

~1780

Do I qualify?Apply below to find out

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Who is running the clinical trial?

Turtle Health, Inc.Lead Sponsor

6 Previous Clinical Trials

230 Total Patients Enrolled

2 Trials studying Infertility

66 Patients Enrolled for Infertility

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the goal of this experiment?

"Turtle Health, Inc., the trial's sponsor, have set a 6-week timeline to measure Image Quality as their primary outcome. As secondary objectives of this study, Turtle are also assessing Ultrasound technologist availability (estimated weekly increase in personnel capacity due to device), Ultrasound technologist satisfaction (difference in average weekly contentment between physical and virtual settings) and Successful Reprocessing (number of probes undergoing reprocessing that are processed properly following internal SOPs)."

Answered by AI

How many candidates are eligible to participate in this medical experiment?

"To ensure that the results of this study are sufficiently robust, Turtle Health Inc. must recruit 1000 individuals who meet the criteria for inclusion in their investigation. These participants will be drawn from two sites; Mayo Clinic located in Rochester, Minnesota and Hospital of the University of Pennsylvania situated in Philadelphia, Pennsylvania."

Answered by AI

Are there opportunities to participate in this clinical research at present?

"Yes, there is evidence on clinicaltrials.gov indicating that this research endeavour is actively searching for participants. It was first announced on July 25th 2022 and has since been updated once; the 1000 individuals necessary must be sourced from 3 distinct locations."

Answered by AI