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NCT00775190 · ClinicalTrials.gov registry record · NA

Side Effect Profiles of Brand Name Versus Generic Oral Contraceptives

A NA study, sponsored by Corewell Health East.

Terminated
Registry status
NA
Development phase
12
Enrollment target

NCT00775190: Clinical Trial NA study, sponsored by Corewell Health East.

NCT00775190 is a NA study that was terminated before completion, run by Corewell Health East. The registered enrollment target is 12 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00775190, a NA study, was terminated before completion, sponsored by Corewell Health East.

TERMINATED
Registry status
NA
Development phase
12 participants
Enrollment target

Study Summary

This is a randomized control trial of Ortho tricyclen versus Trinessa (generic equivalent) to determine if they have similar effects. Women will be randomized to receive either Ortho tricyclen or Trinessa oral contraceptives and will be asked to keep a daily dairy of any symptoms or bleeding experienced. Once a month, participants will be asked to complete a survey. The objective is to compare generic oral contraceptives (OCPs) and brand name OCPs with respect to side effect profiles including bleeding patterns, mood changes, nausea and vomiting, frequency of menstrual cramps, breast tenderness, elevation in blood pressure, stroke, blood clots and patient compliance.

Primary Outcome

Measures how light or heavy the menstrual flow on a 1 to 3 Likert scale. (Light, Medium, Heavy).

Interventions

  • DRUG ortho tricyclen
  • DRUG Trinessa

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2008-10
Est. Completion 2013-11
Phase NA
Corewell Health East

106 total trials

Why NCT00775190 stopped before completion

NCT00775190 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which ortho tricyclen is the first listed.

NCT00775190 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00775190 about?

NCT00775190 is a clinical study titled "Side Effect Profiles of Brand Name Versus Generic Oral Contraceptives". This is a randomized control trial of Ortho tricyclen versus Trinessa (generic equivalent) to determine if they have similar effects. Women will be randomized to receive either Ortho tricyclen or Trinessa oral contraceptives and will be asked to keep a daily dairy of any symptoms or bleeding experie...

What is the current status of trial NCT00775190?

This trial is currently terminated. It is a NA study. The enrollment target is 12 participants. The study started on 2008-10. Estimated completion is 2013-11.

What interventions are being tested in trial NCT00775190?

The interventions under investigation include: ortho tricyclen (DRUG), Trinessa (DRUG).

Who is sponsoring clinical trial NCT00775190?

This trial is sponsored by Corewell Health East, which has 106 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00775190's enrollment target sits among peer trials

12 1913th of 2000 higher than 74 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00775190, the US trial registry maintained by the National Library of Medicine. NCT00775190 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.