Clinical Trial Results:
The exogenous progesterone free luteal phase after GnRHa trigger – a randomized controlled pilot study in normo-responder IVF patients
Summary
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EudraCT number |
2014-000447-32 |
Trial protocol |
DK |
Global end of trial date |
15 Oct 2019
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Results information
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Results version number |
v1(current) |
This version publication date |
17 Dec 2020
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First version publication date |
17 Dec 2020
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Other versions |
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Summary report(s) |
Summary of outcomes |
Trial Information
Subject Disposition
Baseline Characteristics
End Points
Adverse Events
More Information
Subject Disposition
Baseline Characteristics
End Points
Adverse Events
More Information
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Trial identification
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Sponsor protocol code |
Agonist5
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Additional study identifiers
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ISRCTN number |
- | ||
US NCT number |
- | ||
WHO universal trial number (UTN) |
- | ||
Sponsors
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Sponsor organisation name |
The Fertility Clinic Skive
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Sponsor organisation address |
Resenvej 25, ATT. Fertilitetsklinikken, Skive, Denmark, 7800
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Public contact |
Peter humaidan, Skive fertility clinic, +45 78445773, peter.humaidan@midt.rm.dk
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Scientific contact |
Peter humaidan, Skive fertility clinic, 78445760 78445773, peter.humaidan@midt.rm.dk
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Paediatric regulatory details
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Is trial part of an agreed paediatric investigation plan (PIP) |
No
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Does article 45 of REGULATION (EC) No 1901/2006 apply to this trial? |
No
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Does article 46 of REGULATION (EC) No 1901/2006 apply to this trial? |
No
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Results analysis stage
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Analysis stage |
Final
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Date of interim/final analysis |
30 Oct 2020
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Is this the analysis of the primary completion data? |
Yes
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Primary completion date |
15 Oct 2019
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Global end of trial reached? |
Yes
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Global end of trial date |
15 Oct 2019
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Was the trial ended prematurely? |
No
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General information about the trial
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Main objective of the trial |
The objective of this pilot RCT is to explore the exogenous progesterone-free luteal phase support after GnRHa trigger in a population of IVF patients without imminent risk of OHSS development compared with a control group who will receive hCG.
The primary end-point will be the reproductive outcome defined as the ongoing pregnancy rate per patient at 10th week of gestation.
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Protection of trial subjects |
The study was approved by the scientific Ethics Committee of the Central Denmark Region – Project
number: M201337713.
Written informed consent was obtained from all participants prior to inclusion.
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Background therapy |
- | ||
Evidence for comparator |
- | ||
Actual start date of recruitment |
03 Mar 2014
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Long term follow-up planned |
No
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Independent data monitoring committee (IDMC) involvement? |
Yes
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Population of trial subjects
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Number of subjects enrolled per country |
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Country: Number of subjects enrolled |
Denmark: 130
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Worldwide total number of subjects |
130
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EEA total number of subjects |
130
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Number of subjects enrolled per age group |
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In utero |
0
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Preterm newborn - gestational age < 37 wk |
0
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Newborns (0-27 days) |
0
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Infants and toddlers (28 days-23 months) |
0
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Children (2-11 years) |
0
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Adolescents (12-17 years) |
0
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Adults (18-64 years) |
130
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From 65 to 84 years |
0
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85 years and over |
0
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Recruitment
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Recruitment details |
The first patient was enrolled in November 2014 and the last patient was enrolled in August 2019. All patients were from The fertility clinic, Skive Regional Hospital, Denmark. | |||||||||||||||
Pre-assignment
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Screening details |
A total of 275 IVF patients were assessed for eligibility and 250 patients were subsequently recruited for two studies, 2014-000448-13 and 2014-000447-32. 120 patients were randomized in 2014-000448-13 and 130 patients were randomized in 2014-000447-32. No patient was lost to follow-up. | |||||||||||||||
Period 1
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Period 1 title |
Overall period
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Is this the baseline period? |
Yes | |||||||||||||||
Allocation method |
Randomised - controlled
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Blinding used |
Not blinded | |||||||||||||||
Arms
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Are arms mutually exclusive |
Yes
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Arm title
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GnRHa trigger | |||||||||||||||
Arm description |
Ovulation trigger with a bolus of 0.5 mg Buserelin (Suprefact®, Sanofi A/S, Copenhagen, Denmark), followed by a bolus of 1500 IU hCG (Pregnyl®, MSD, Skovlunde, Denmark) after OR and an additional bolus of 1000 IU hCG (Pregnyl®) on OR + 4 days. | |||||||||||||||
Arm type |
Experimental | |||||||||||||||
Investigational medicinal product name |
Buserelin
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Investigational medicinal product code |
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Other name |
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Pharmaceutical forms |
Concentrate for solution for injection
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Routes of administration |
Subcutaneous use
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Dosage and administration details |
Trigger with a bolus of 0.5 mg Buserelin (Suprefact®, Sanofi A/S, Copenhagen, Denmark), followed by a bolus of 1500 IU hCG (Pregnyl®, MSD, Skovlunde, Denmark) after OR and an additional bolus of 1000 IU hCG (Pregnyl®) on OR + 4 days.
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Arm title
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hCG trigger | |||||||||||||||
Arm description |
trigger with 6500 IU hCG (Ovitrelle®) followed by 100 mg vaginal progesterone (Lutinus®, Ferring, Copenhagen, Denmark) three times daily until the pregnancy test (14 days after OR), after which LPS was stopped. | |||||||||||||||
Arm type |
Active comparator | |||||||||||||||
Investigational medicinal product name |
Ovitrelle
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Investigational medicinal product code |
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Other name |
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Pharmaceutical forms |
Concentrate for solution for injection
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Routes of administration |
Subcutaneous use
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Dosage and administration details |
Trigger with 6500 IU hCG (Ovitrelle®) followed by 100 mg vaginal progesterone (Lutinus®, Ferring, Copenhagen, Denmark) three times daily until the pregnancy test (14 days after OR), after which LPS was stopped.
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Baseline characteristics reporting groups
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Reporting group title |
Overall period
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Reporting group description |
- | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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End points reporting groups
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Reporting group title |
GnRHa trigger
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Reporting group description |
Ovulation trigger with a bolus of 0.5 mg Buserelin (Suprefact®, Sanofi A/S, Copenhagen, Denmark), followed by a bolus of 1500 IU hCG (Pregnyl®, MSD, Skovlunde, Denmark) after OR and an additional bolus of 1000 IU hCG (Pregnyl®) on OR + 4 days. | ||
Reporting group title |
hCG trigger
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Reporting group description |
trigger with 6500 IU hCG (Ovitrelle®) followed by 100 mg vaginal progesterone (Lutinus®, Ferring, Copenhagen, Denmark) three times daily until the pregnancy test (14 days after OR), after which LPS was stopped. | ||
Subject analysis set title |
modified intention to treat analysis
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Subject analysis set type |
Modified intention-to-treat | ||
Subject analysis set description |
The primary analysis was the modified intention to treat analysis (White et al., 2011) of all randomized
patients having an embryo transfer under the assumption that missing outcome data (patients not
having an embryo transfer) was missing conditionally at random.
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End point title |
Ongoing pregnancy | ||||||||||||
End point description |
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End point type |
Primary
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End point timeframe |
12 weeks
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Statistical analysis title |
Binary regression | ||||||||||||
Statistical analysis description |
A binary regression model was used to calculate the crude relative risks and relative differences (cRR,
cRD) and adjusted relative risks and relative differences (aRR, aRD) for the primary outcome.
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Comparison groups |
GnRHa trigger v hCG trigger v modified intention to treat analysis
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Number of subjects included in analysis |
208
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Analysis specification |
Pre-specified
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Analysis type |
equivalence | ||||||||||||
P-value |
< 0.05 | ||||||||||||
Method |
Regression, Linear | ||||||||||||
Parameter type |
Risk ratio (RR) | ||||||||||||
Point estimate |
0.95
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Confidence interval |
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level |
95% | ||||||||||||
sides |
2-sided
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lower limit |
0.62 | ||||||||||||
upper limit |
1.45 |
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Adverse events information [1]
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Timeframe for reporting adverse events |
14 weeks
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Adverse event reporting additional description |
We did not collect adverse events systematically
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Assessment type |
Non-systematic | ||
Dictionary used for adverse event reporting
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Dictionary name |
MedDRA | ||
Dictionary version |
23
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Frequency threshold for reporting non-serious adverse events: 5% | |||
Notes [1] - There are no non-serious adverse events recorded for these results. It is expected that there will be at least one non-serious adverse event reported. Justification: We did not systematically collect adverse events. Ovarian hyperstimulation syndrome will be reported in the publication already submitted to an international journal |
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Substantial protocol amendments (globally) |
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Were there any global substantial amendments to the protocol? No | |||
Interruptions (globally) |
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Were there any global interruptions to the trial? No | |||
Limitations and caveats |
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Limitations of the trial such as small numbers of subjects analysed or technical problems leading to unreliable data. | |||
Sample size and no blinding. |