ClinicalTrials.gg
CompletedNCT02710981Updated May 5, 2020Results posted

Sildenafil Vaginal Gel Co-treatment With Clomiphene Citrate in Infertile Women With Thin Endometrium

An interventional study of clomiphene citrate and Sildenafil vaginal gel in Anovulation, sponsored by Assiut University. Completed. Open to female participants aged 20 Years to 40 Years. Per ClinicalTrials.gov, last updated 2020-05-05.

Sponsored by Assiut University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
42
Allocation
Non-randomized
Ages
20 Years to 40 Years
Sex
Female
01

Study summary

This is a prospective self controlled clinical trial. Women with clomiphene Citrate failure, and thin endometrium were recruited (N = 42). In their 6th (Clomiphene citrate only) cycle, women continued on Clomiphene citrate 100 mg/ day for 5 days, and had sonographic measurement of their endometrial thickness , and Doppler evaluation of their uterine arteries on the day of HCG administration. In 7th cycle, women (N = 36) were given usual dose of Clomiphene citrate supplemented with sildenafil vagina gel (5 gm, containing 50 mg sildenafil) twice daily from cycle day 8 till the day of HCG injection. Endometrial thickness and uterine artery Doppler were measured on the day of HCG administration.

Read the detailed description

Study design:

This is a prospective self-controlled clinical trial.

Study subjects:

Investigators counseled and recruited 42 infertile women who had been diagnosed with anovulatory infertility, with normal baseline FSH, LH, and free testosterone levels, patent tubes on hysterosalpingography, and normal male semen analysis.

By the time they were enrolled in the study, all women had already completed 5 ovulatory cycles of Clomiphene citrate induction (in a dose of 100 mg/ day in two divided doses starting from day 3 of the cycle for 5 days) but without conception (clomiphene citrate failure) with thin endometrium (\<8mm) in at least 3 cycles. Ovulation was documented sonographically, and with day-21 serum progesterone exceeding 5 ng/ ml in all cases.

Exclusion criteria:

Women with major medical problems, male factor infertility, endocrine abnormalities such as hyperprolactinemia or abnormal thyroid functions, prior ovarian or adnexal surgery, or organic pelvic pathology were not included in the study.

Intervention:

Sixth cycle (Clomiphene citrate only):

Enrolled cases were asked to continue with Clomiphene citrate induction ( at the same dose) for the 6th cycle. A gel base, without medicament (vehicle only), was applied vaginally in a dose of 5 gm twice per day, from cycle day 8 to the day of HCG administration ( when follicular diameter reached 18 mm). Endometrial thickness and Uterine artery Doppler assessment were done in the late proliferative phase ( Day of HCG injection).

Seventh cycle ( Sildenafil vaginal gel and Clomiphene cycle):

Those who didn't conceive on the sixth cycle (41 women) were asked to have an extra (7th) cycle in which they were prescribed the usual dose of Clomiphene citrate in addition to sildenafil vaginal gel. The sildenafil vaginal gel consists of sildenafil acetate as a medicament loaded on an in situ gelling system based on two polymers: Pluronic p-127, and Hydroxy Ethyl Cellulose. The dose was 5 g gel containing 50 mg sildenafil, applied vaginally twice daily from cycle day 8 to Day of HCG injection. The gel was prepared in collaboration with the department of pharmaceutics, faculty of Pharmacy, Assiut University. Sixty grams of gel were prepared in tubes and every patient was given 10 applicators like that used for administration of vaginal antimycotic creams to use them for applying the gel.

Evaluation of the study end points:

On day of HCG injection (main follicular diameter of 18 mm) in the 6th, and 7th cycles, women came for follow up and had transvaginal sonographic assessment of their endometrial thickness. Investigators have measured the maximal distance spanning endometrial- myometrial interphase on each endometrial stripe in a sagittal plane in the fundus of the uterus. In addition, Transvaginal Doppler examination was also done on the same visit to evaluate the pulsatility indices of both uterine arteries. When the leading follicle reached 18 mm in diameter, 5000 IU of HCG was prescribed for IM injection.

Although pregnancy rate was not a primary outcome measure in the study, investigators detected pregnancy in 3 cases in the cohort of 36 cases of infertile women with clomiphene failure in which sildenafil gel was added as an adjuvant. Pregnancy was diagnosed with a B-HCG value above 100 mIU/ml, and confirmed later with ultrasound.

Statistics:

Data were analyzed using SPSS program ver. 17 using Student-t-test and Fisher's exact test for comparing data in the 6th and 7th cycles, as appropriate.

02

Conditions studied

  • Anovulation

Browse trials for

Keywords

  • Sildenafil vaginal gel
  • endometrium
  • clomiphene
  • anovulation
03

In context

Anovulation

75 studies on the registry are indexed under Anovulation; 7 are open to participants now.

This study's enrollment of 42 is below the median of 80 across 52 interventional studies indexed under Anovulation.

Browse Anovulation studies →

Lead sponsor

Assiut University is the lead sponsor of 5,078 studies on the registry; 2,178 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 40 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Women with clomiphene citrate failure (defined as at least prior 5 ovulatory cycles with clomiphene citrate, with no conception),
  • persistently thin endometrium (less than 8 mm in at least 3 cycles).
  • normal baseline FSH, LH, and free testosterone levels, patent tubes on hysterosalpingography, and normal male semen analysis

Exclusion criteria

Exclusion Criteria:

  • Women with major medical problems,
  • male factor infertility,
  • endocrine abnormalities such as hyperprolactinemia or abnormal thyroid functions,
  • prior ovarian or adnexal surgery, or organic pelvic pathology
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
42 participants (actual)

Study arms

  • Active comparator
    Clomiphene citrate only

    women with prior 5 ovulatory cycles of Clomiphene citrate induction, but without conception (clomiphene citrate failure), with thin endometrium (\<8mm) in at least 3 cycles.

    Drug: clomiphene citrate

  • Experimental
    Sildenafil vaginal gel and Clomiphene

    Women who did not conceive on the Clomiphene citrate only cycle (41 women) were given Clomiphene citrate 100 mg/ day starting from day of the cycle for 5 days, with the addition to sildenafil vaginal gel 5 gm twice daily starting from day 8 of the cycle until day of HCG injection.

    Drug: clomiphene citrate · Drug: Sildenafil vaginal gel

Interventions

  • Clomiphene citrate only arm: Patients received Clomiphene citrate induction ( (in a dose of 100 mg/ day in two divided doses starting from day 3 of the cycle for 5 days) for the 6th cycle. A gel base, without medicament (vehicle only), was applied vaginally in a dose of 5 gm twice per day, from cycle day 8 to the day of HCG injection. Sonographic assessment of endometrial thickness together with Uterine artery Doppler evaluation were done in the late proliferative phase ( Day of HCG injection).

    Also known as: clomid only

  • In addition to clomiphene citrate treatment as the previous group, women in the second arm were prescribed sildenafil vaginal gel in a dose of 5 g gel applied vaginally twice daily from cycle day 8 to the day of HCG injection. The sildenafil vaginal gel consists of sildenafil acetate as a medicament loaded on an in situ gelling system based on two polymers: Pluronic p-127, and Hydroxy Ethyl Cellulose.The gel was prepared in collaboration with the department of pharmaceutics, faculty of Pharmacy, Assiut University. Sixty grams of gel were prepared in tubes and every patient was given 10 applicators like that used for administration of vaginal antimycotic creams to use them for applying the gel.

    Also known as: Viagra vaginal gel

06

What researchers measure

Primary outcomes

  1. Endometrial Thickness

    Transvaginal sonographic measurement of maximal distance spanning endometrial- myometrial interphase on each endometrial stripe in a sagittal plane in the fundus of the uterus

    Time frame: Day of HCG administration

Secondary outcomes

  1. Uterine Blood Flow

    Doppler ultrasound is used to measure the pulsatility index in both uterine arteries. Pulsatility index is a measure of the arterial resistance to blood flow. The higher the value of the pulsatility index, the more resistant the uterine arteries are, and hence the worst the outcome.

    Time frame: Day of HCG administration

  2. Clinical Pregnancy Rate

    Identifying pregnancy through positive urinary HCG test plus sonographic detection of cardiac pulsations

    Time frame: At the end of a 28-day menstrual cycle.

07

Results

Posted May 5, 2020

Participant flow

6th Ovulation Induction Cycle (5 Days)
Participant flow — 6th Ovulation Induction Cycle (5 Days)
MilestoneClomiphene Citrate OnlyClomiphene Citrate Plus Sildenafil Vaginal Gel (7th Ovulation)
Started420
Completed410
Not completed10
7th Ovulation Induction Cycle (5 Days)
Participant flow — 7th Ovulation Induction Cycle (5 Days)
MilestoneClomiphene Citrate OnlyClomiphene Citrate Plus Sildenafil Vaginal Gel (7th Ovulation)
Started041
Completed036
Not completed05

Outcome measures

PrimaryEndometrial Thickness

Transvaginal sonographic measurement of maximal distance spanning endometrial- myometrial interphase on each endometrial stripe in a sagittal plane in the fundus of the uterus

Time frame:
Day of HCG administration
Reported as:
Mean · millimeter
Endometrial Thickness
millimeterClomiphene Citrate Only Group (6th Ovulation Induction Cycle)Clomiphene Citrate Plus Sildenafil Vaginal Gel (7th Ovulation)
Endometrial Thickness6.6 ± 1.49.3 ± 3.1
SecondaryUterine Blood Flow

Doppler ultrasound is used to measure the pulsatility index in both uterine arteries. Pulsatility index is a measure of the arterial resistance to blood flow. The higher the value of the pulsatility index, the more resistant the uterine arteries are, and hence the worst the outcome.

Time frame:
Day of HCG administration
Reported as:
Mean · index
Uterine Blood Flow
indexClomiphene Citrate Only Group (6th Ovulation Induction Cycle)Clomiphene Citrate Plus Sildenafil Vaginal Gel (7th Ovulation)
Uterine Blood Flow2.4 ± 0.81.6 ± 1.3
SecondaryClinical Pregnancy Rate

Identifying pregnancy through positive urinary HCG test plus sonographic detection of cardiac pulsations

Time frame:
At the end of a 28-day menstrual cycle.
Reported as:
Count of participants · Participants
Clinical Pregnancy Rate
ParticipantsClomiphene Citrate Only Group (6th Ovulation Induction Cycle)Clomiphene Citrate Plus Sildenafil Vaginal Gel (7th Ovulation
Clinical Pregnancy Rate03

Adverse events

Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Clomiphene Citrate Only Group (6th Ovulation Induction Cycle)—0/42 (0%)0/41 (0%)
Clomiphene Citrate Plus Sildenafil Vaginal Gel (7th Ovulation)—0/41 (0%)1/36 (2.8%)
Most frequent other events
Most frequent other events
EventClomiphene Citrate Only Group (6th Ovulation Induction Cycle)Clomiphene Citrate Plus Sildenafil Vaginal Gel (7th Ovulation)
Vasodilatory headacheVascular disorders0/411/36

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Clomiphene Citrate Only Group (6th Ovulation Induction Cycle)
<=18 years0
Between 18 and 65 years41
>=65 years0
Age, Continuous
Age, Continuous(years)Clomiphene Citrate Only Group (6th Ovulation Induction Cycle)
Mean26.8 ± 2.8
Sex: Female, Male
Sex: Female, Male(Participants)Clomiphene Citrate Only Group (6th Ovulation Induction Cycle)
Female41
Male0
Race and Ethnicity Not Collected
Race and Ethnicity Not Collected(Participants)Clomiphene Citrate Only Group (6th Ovulation Induction Cycle)
Region of Enrollment
Region of Enrollment(participants)Clomiphene Citrate Only Group (6th Ovulation Induction Cycle)
Egypt41
Serum FSH
Serum FSH(U/L)Clomiphene Citrate Only Group (6th Ovulation Induction Cycle)
Mean4.5 ± 1.5
08

Study locations

No study locations are listed for this record.

09

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

10

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jun 2015, a primary completion of Jan 2016 and a completion of Jan 2016. It does not say whether these dates are actual or estimated.

Results were first posted in May 2020, 4 years 4 months after primary completion.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 4, 2016
First posted
Mar 17, 2016
Start
Jun 2015
Primary completionActual
Jan 2016
CompletionActual
Jan 2016
Results first posted
May 5, 2020
Last update
May 5, 2020
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 5, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT02710981
Lead sponsor
Assiut University
Responsible party
Essam Rashad Abdel-Hafeez Othman (Associate professor, Assiut University) — Principal investigator
First posted
Mar 17, 2016
Start date
Jun 2015
Primary completion
Jan 2016
Completion
Jan 2016
Results posted
May 5, 2020
Last update
May 5, 2020

Study contacts

Ahmed N. Fetih, M.D.
study director · Assiut University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2020. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Studies of the drug tested here: Sildenafil

Start the discussion