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Comparison of Triggers in Double Ovarian Stimulation (DuoStim).

Double Ovarian Stimulation (DuoStim) Comparison of Triggers: Is There Any Advantage Using 3 Different Methods of Trigger for the Second Egg Collection in Predicted Low Responders?

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05321511
Acronym
COTRID
Enrollment
165
Registered
2022-04-11
Start date
2022-03-03
Completion date
2023-03-31
Last updated
2022-04-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

IVF, LOW OVARIAN RESPONSE

Brief summary

This study aims to investigate the efficacy of 3 different trigggers used for final maturation in the second ovarian stimulation in double stimulation protocol (aGnRH and hCG-rec vs. aGnRH only vs. hCG-rec only). The main objective is to compare the number of all retrieved oocytes and mature oocytes in patients predicted to be low ovarian responders. This is a controlled randomized clinical study where 165 patients will be recruited.

Interventions

DRUGTriptorelin acetate (a-GnRH)

Adminsitration of triptoreline acetate 0.2 mg for final oocyte maturation in the second ovarian stimuation inthe Double stimulation protocol.

DRUGOvitrelle® (hCG)

Adminsitration of coriogonadotropine alfa 250 mcg for final oocyte maturation in the second ovarian stimuation inthe Double stimulation protocol.

DRUGDecapeptyl 0.1 mg® (a-GnRH) and Ovitrelle® (hCG) used together

Adminsitration of triptoreline acetate 0.2 mg and coriogonadotropine alfa 250 mcg for final oocyte maturation in the second ovarian stimuation inthe Double stimulation protocol.

Sponsors

Instituto Bernabeu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
28 Years to 43 Years
Healthy volunteers
Yes

Inclusion criteria

* BMI below 32 * Presence of both ovaries * Indication for ovarian stimulation under Double Stimulation protocol (Duo Stim) * Meeting the criteria for Duo Stim * Medical history, history and physical examination without alterations * AMH and AFV results in accordnace to Poseidon classification group 3 or 4 no more than 6 months prior to signing the consent form * Ability to participate and comply with the study protocol. * To have given written consent * Normal karyotype and fragile X.

Exclusion criteria

* Non-compliance with instructions and/or non-formalization of consents or legal requirements for IVF. * Concurrent participation in another study

Design outcomes

Primary

MeasureTime frameDescription
number of retrieved oocytesthrough study completion, usually will be evaluated on the last day of the treatmentnumber of oocytes retrieved in the second ovarian stimulation in the double stimulation protocol.
number of mature (MII) oocytesthrough study completion, usually will be evaluated on the last day of the treatmentnumber of mature (MII) oocytes retrieved in the second ovarian stimulation in the double stimulation protocol.

Countries

Spain

Contacts

Primary ContactAnna Pitas, PhD
apitas@institutobernabeu.com+34663926079

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026