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Trial registered on ANZCTR


Registration number
ACTRN12614000657628
Ethics application status
Approved
Date submitted
10/06/2014
Date registered
24/06/2014
Date last updated
10/05/2022
Date data sharing statement initially provided
26/11/2018
Date results provided
26/02/2021
Type of registration
Prospectively registered

Titles & IDs
Public title
Pipelle for pregnancy in couples with subfertility related to polycystic ovarian syndrome
Scientific title
A single-blind, randomised controlled trial assessing the effect of endometrial pipelle biopsy vs. sham biopsy on live birth rate in couples with subfertility related to polycystic ovarian syndrome
Secondary ID [1] 284679 0
nil
Universal Trial Number (UTN)
U111111556458
Trial acronym
PIP-PCOS
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Polycystic ovarian syndrome 292019 0
Condition category
Condition code
Reproductive Health and Childbirth 292365 292365 0 0
Fertility including in vitro fertilisation

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Women will undergo a single endometrial pipelle biopsy performed between days 1 and 12 of a stimulated cycle (clomiphene, letrozole or metformin).
Intervention code [1] 289464 0
Treatment: Other
Comparator / control treatment
Women will undergo a single endometrial sham biopsy (the biopsy cannula will be placed at the anterior fornix and not inserted into the uterus). This procedure will be performed between days 1 and 12 of a stimulated cycle (clomiphene, letrozole or metformin).
Control group
Placebo

Outcomes
Primary outcome [1] 292220 0
Live birth - delivery of a live infant at least 20 weeks gestation
Timepoint [1] 292220 0
Approximately 9 months following the end of the study period
Secondary outcome [1] 308449 0
Clinical pregnancy - on ultrasound, the presence of at least one gestational sac
Timepoint [1] 308449 0
6 weeks following each ovulation induction cycle (3 consecutive ovulation induction cycles, unless pregnancy occurs)
Secondary outcome [2] 308450 0
Ongoing pregnancy - on ultrasound, the presence of at least one gestational sac and heartbeat
Timepoint [2] 308450 0
12 weeks following each ovulation induction cycle (3 consecutive ovulation induction cycles, unless pregnancy occurs)
Secondary outcome [3] 308451 0
Multiple pregnancy - on ultrasound, the presence of more than one heartbeat
Timepoint [3] 308451 0
6 weeks following each ovulation induction cycle (3 consecutive ovulation induction cycles, unless pregnancy occurs)
Secondary outcome [4] 308452 0
Adverse events - including miscarriage, ectopic pregnancy, pain or bleeding following the procedure, infection etc.
Timepoint [4] 308452 0
Bleeding and pain: on the day of the procedure or the following day
Infection: for 1 month following the procedure
Ectopic pregnancy and miscarriage: up to 20 weeks following the cycle in which pregnancy occurs

Eligibility
Key inclusion criteria
1. Couples having regular unprotected sexual intercourse in a relationship where pregnancy is desired
2. Women is between 18-42 years of age at the time of randomisation
3. Women who meet the criteria for PCOS, at least two of the following: 1) oligoovulation or anovulation (progesterone test) 2) excess androgen activity (elevated serum testosterone or clinical signs such as excess hair), 3) polycystic ovaries (as evidenced on ultrasound) – as per the Rotterdam criteria
4. Have either a) two ovaries and two probably patent fallopian tube (confirmed by hysteroscopy or HSG - one tube may spasm/not free spill). b) been ovulating on ovulation induction mediction for 6 months or less (as HSG may not be recommended until failure to achieve pregnancy following three or more cycles of successful ovulation), or c) A previous intrauterine pregnancy, and no subsequent surgery or ectopic pregnancy that may reduce tubal patency or ovarian function
5. A body mass index (BMI) less than or equal to 35
6. Have a negative cervical PAP smear within the last 3 years
7. Be willing to have regular sexual intercourse following the procedure in the month of the procedure, and for two months following the procedure (or until pregnancy occurs). For PCOS women, this includes three months of consecutive ovulation induction (unless pregnancy occurs)
8. Be willing to remain on ovulation induction medication for the study period (unless pregnancy occurs), either: clomiphene, letrozole or metformin (or a combination). Doses may vary.
9. Women who’s male partner has normal semen analysis (volume at least 1.5ml, progressive motility at least 32%, concentration at least 15million/ml) or a total motile count of equal to or more than 10 million
Minimum age
18 Years
Maximum age
42 Years
Sex
Females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Have had any disruptive instrumentation within the uterine cavity (e.g. hysteroscopy, hysterosalpingogram, laparoscopy, surgically managed miscarriage or endometrial biopsy) within three months prior to day one of the planned ovulation induction cycle, or planning to undergo a procedure involving disruptive instrumentation at any stage during the study.
2. The presence of any other cause of infertility, where spontaneous conception is unlikely (e.g. large fibroids)
3. Recurrent miscarriage
4. Entered previously into this study or participation in another trial in the last 30 days
5. Any contraindication to endometrial biopsy or being pregnant and/or carrying a pregnancy to term

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
To ensure allocation concealment, randomisation of eligible individuals will be performed by an online randomisation system built into the data collection software.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
A computer generated block randomisation schedule, stratified for each fertility centre, will be created and protected by the database manager
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
1/07/2014
Actual
27/06/2014
Date of last participant enrolment
Anticipated
Actual
31/12/2019
Date of last data collection
Anticipated
Actual
31/12/2020
Sample size
Target
280
Accrual to date
Final
117
Recruitment outside Australia
Country [1] 6101 0
Brazil
State/province [1] 6101 0
Country [2] 7359 0
Egypt
State/province [2] 7359 0
Cairo
Country [3] 21070 0
New Zealand
State/province [3] 21070 0
Country [4] 21071 0
United Kingdom
State/province [4] 21071 0

Funding & Sponsors
Funding source category [1] 289365 0
Hospital
Name [1] 289365 0
Auckland District Health Board
Country [1] 289365 0
New Zealand
Primary sponsor type
Hospital
Name
Auckland District Health Board
Address
Bldg 14, Greenlane Clinical Centre Level 7/214 Green Ln W, Greenlane 1051
Country
New Zealand
Secondary sponsor category [1] 288050 0
None
Name [1] 288050 0
Address [1] 288050 0
Country [1] 288050 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 291131 0
Northern A Health and Disability Ethics Committee
Ethics committee address [1] 291131 0
Ethics committee country [1] 291131 0
New Zealand
Date submitted for ethics approval [1] 291131 0
29/04/2014
Approval date [1] 291131 0
06/06/2014
Ethics approval number [1] 291131 0
14/NTA/62

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 48750 0
Prof Cynthia Farquhar
Address 48750 0
Department of Obstetrics and Gynaecology and National Women's Health, University of Auckland, Level 12, ACH Support Building, Auckland City Hospital, Park Road, Grafton Private Bag 92019 Auckland 1020
Country 48750 0
New Zealand
Phone 48750 0
+64 9 3737599 EXT 89493
Fax 48750 0
Email 48750 0
[email protected]
Contact person for public queries
Name 48751 0
Sarah Lensen
Address 48751 0
Department of Obstetrics and Gynaecology and National Women's Health, University of Auckland, Level 12, ACH Support Building, Auckland City Hospital, Park Road, Grafton Private Bag 92019 Auckland 1020
Country 48751 0
New Zealand
Phone 48751 0
+64 9 3737599 EXT 89487
Fax 48751 0
Email 48751 0
[email protected]
Contact person for scientific queries
Name 48752 0
Cynthia Farquhar
Address 48752 0
Department of Obstetrics and Gynaecology and National Women's Health, University of Auckland, Level 12, ACH Support Building, Auckland City Hospital, Park Road, Grafton Private Bag 92019 Auckland 1020
Country 48752 0
New Zealand
Phone 48752 0
+64 9 3737599 EXT 89493
Fax 48752 0
Email 48752 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
What data in particular will be shared?
All IPD, anonymised
When will data be available (start and end dates)?
After data analysis for the primary study; approx mid 2021. IPD will be available for at least 5 years after this date, no end date determined
Available to whom?
Researchers with bonafide research questions, e.g. IPD projects
Available for what types of analyses?
Variable
How or where can data be obtained?
By sending an email request to [email protected]


What supporting documents are/will be available?

Doc. No.TypeCitationLinkEmailOther DetailsAttachment
10820Study protocolDOI 10.1186/s13063-016-1301-9https://trialsjournal.biomedcentral.com/track/pdf/10.1186/s13063-016-1301-9[email protected] Na 366423-(Uploaded-27-07-2020-09-02-26)-Study-related document.pdf



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
SourceTitleYear of PublicationDOI
EmbaseA randomized trial of endometrial scratching in women with PCOS undergoing ovulation induction cycles.2022https://dx.doi.org/10.1016/j.rbmo.2021.10.008
N.B. These documents automatically identified may not have been verified by the study sponsor.