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NCT04644380

Assessment of the INVOcell Culture Device When Used for up to Five-Day Incubation

Completed NA Last updated 17 February 2021
What this trial tests

NA trial testing INVOcell in Infertility in 31 participants. Completed in 11 December 2020.

Timeline
2 December 2020
Primary endpoint
11 December 2020
11 December 2020

Quick facts

Lead sponsorINVO Bioscience, Inc.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment31
Start date2 December 2020
Primary completion11 December 2020
Estimated completion11 December 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

INVO Bioscience, Inc.

Who can join

Adults 18 to 42, female only, with Infertility. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The INVOcell Culture Device received de novo request for 3-day intravaginal incubation. The device is held in place with the intravaginal cavity by a Retention Device. The clinical study will assess the ability of a modified Retention Device to hold INVOcell in place during 5-day vaginal incubation as well as comfort and vaginal irritation as secondary endpoints.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Infertility

Currently open trials in the same condition.

Other INVO Bioscience, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04644380.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing