Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This is a clinical study designed to validate the usability and safety of the over-the-counter (OTC) device by obtaining feedback in a home use environment regarding ease of use of The Stork™ Conception System and the instructions for use. In addition to usability, results for safety, including vaginal
Female participants will undergo a baseline pelvic examination. Participating couples will be given The Stork™ Conception System (OTC), including Instructions for Use, the questionnaire and two ziplock bags. The device will be used in accordance with the instructions for use. Participants will use the Conceptacle as a collection condom during sexual intercourse. Participants will remove the Cervical Cap from the Sheath of the Conceptacle and discard the Sheath. Participants will then load the Cervical Cap into the Applicator for insertion, placement and deployment of the device. Participants will wash the applicator with soap and water and place it in the double zip lock bags. During the time the cervical cap is inserted, normal activity will be recommended with the exception of having intercourse. The female participants will leave the conception cap inserted for a period of time between 4 and 12 hours, return to the investigator's office for examination, remove the Cervical Cap, and undergo a follow up pelvic examination. Participants will be asked to complete the study and the questionnaire within 3 days of receiving the study packet. As a result, this study could take up to 4 days to complete per enrolled couple.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| The Stork | No Intervention | Device - The Stork - complete kit (Conceptacle and Applicator) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| The Stork - Conception Aid | Device |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Efficacy -Primary endpoint part 1 - Collection | The primary endpoint of the study is comprised of 3 parts. It is binary, in the sense that if all of the three parts are "passed" then the endpoint is met for that couple. If any part of the endpoint is not met then the endpoint for that couple is not met. The three parts of the endpoint are: P1: Participants indicate ability to collect and contain semen using the Conceptacle™. The examinations will occur 4-12 hours after device insertion. | 1-3 days |
| Efficacy - Primary endpoint part 2 - Placement | The primary endpoint of the study is comprised of 3 parts. It is binary, in the sense that if all of the three parts are "passed" then the endpoint is met for that couple. If any part of the endpoint is not met then the endpoint for that couple is not met. P2: Successful placement of the cervical cap as determined by physical examination. | 4-12 hrs |
| Primary endpoint part 3 -Safety | The primary endpoint of the study is comprised of 3 parts. It is binary, in the sense that if all of the three parts are "passed" then the endpoint is met for that couple. If any part of the endpoint is not met then the endpoint for that couple is not met. P3: Participants use the device without any evidence of damage to the female participants' genital tract as depicted by physician examination. | 4-12 hrs |
| Measure | Description | Time Frame |
|---|---|---|
| Secondary Endpoint | Secondary Objectives: Pass/Fail Answers to the specific questions Male 1-3 and Female 1-4 on the CRF will be compiled descriptively to indicate participant success during the study. | up to 3 days |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Michael J Pelekanos, OB-GYN | Forbes Regional Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Forbes Regional Hospital | Monroeville | Pennsylvania | 15146 | United States |
| Type | Date | Date Unknown |
|---|---|---|
| Release | May 7, 2015 | |
| Reset | May 22, 2015 | |
| Release | Oct 19, 2015 | |
| Reset | Nov 18, 2015 | |
| Release | Sep 26, 2016 | |
| Reset | Nov 14, 2016 | |
| Release | May 9, 2017 | |
| Reset | Jun 9, 2017 |
Not provided
Not provided
| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| May 7, 2015 | May 22, 2015 | |||
| Oct 19, 2015 |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Nov 18, 2015 |
| Sep 26, 2016 | Nov 14, 2016 |
| May 9, 2017 | Jun 9, 2017 |