Live Birth After Additional Tubal Flushing With Oil-based Contrast Versus no Additional Flushing:

NCT04379973 | Active Not Recruiting Phase 4

• 1 other identifier: HYOIL
• Study Type: interventional
• Target: 736
• Locations: 1 country
• Sites: 16

Brief Summary

Ten to 15 percent of couples in their reproductive lifetime face fertility problems which is defined by WHO as the absence of pregnancy after minimal 12 months of unprotected sexual intercourse. The three most frequent causes of subfertility are: sperm defects, ovulation disorders and tubal pathology. In order to exclude tubal pathology, tubal patency tests are performed under ultrasound guidance with foam (hysterosalpingo-foam sonography (Hyfosy)) or with contrast/water (hysterosalpingo-contrast sonography (Hycosy)). This trial will investigate whether tubal flushing with an oil-soluble contrast medium (OSCM) can increase the likelihood of a spontaneous conception after tubal patency testing with Hyfosy under ultrasound guidance compared to no additional flushing in a population of infertile women between 18 and 40 years of age with absence of pregnancy after 12 months of unprotected sexual intercourse or who have three cycles of donor insemination without pregnancy or three ovulatory ovulation induction cycles without pregnancy. The use of Lipiodol Ultra Fluide® is off-label in Hyfosy. This multicenter, randomised, open-label, comparative and pragmatic trial compares 2 arms which will be randomised 1:1:

• Intervention group: Tubal flush with 5-10mL oil-soluble contrast medium (Lipiodol Ultra Fluide®, Guerbet, France) immediately after Hyfosy
• Control group: No additional intervention after Hyfosy The study comprises a screening period of maximum 8 weeks (w-8 to d1), randomisation (w-8 to d1), a start study visit at which the Hyfosy is performed (d1) and a fertility treatment period of 6 months (d1-w26). If the woman is not pregnant at 6 months after Hyfosy, the follow-up will last till 12 months (w52). If the participant is pregnant at 6 months after Hyfosy, the follow-up will last till maximal 4 months after live birth or miscarriage. The primary endpoint is the occurrence of live birth, with the first day of the last menstrual cycle in which the patient conceives within 6 months after Hyfosy. Secondary endpoints consist of reproductive outcomes, gestational age at delivery, birth weight, neonatal mortality, major congenital anomaly, neonatal outcomes and thyroid function, pregnancy complications, number of complications during or immediately after the intervention, pain score of the Hyfosy and additional flush, thyroid function of the mother, general and disease-specific quality of life.

Conditions

Infertility, Female

Outcome Measures

Primary Outcomes (1)

• Live birth

  the occurrence of live birth, counting from the first day of the last menstrual cycle in which the patient conceives within 6 months after Hyfosy.

  Delivery

Secondary Outcomes (19)

• Type of pregnancy

  15 months after Hyfosy

• Number of miscarriages

  15 months after Hyfosy

• Amount of pregnancy complications

  15 months after Hyfosy

• Number of ectopic pregnancies

  15 months after Hyfosy

• Number of clinical pregnancies

  15 months after Hyfosy

Study Arms (2)

Tubal flush with Lipiodol Ultra Fluide® after Hyfosy

EXPERIMENTAL

Drug: Lipiodol Ultra Fluide®

No tubal flush after Hyfosy

NO INTERVENTION

Interventions

Lipiodol Ultra Fluide® DRUG

Tubal flush with 5-10mL oil-soluble contrast medium (OSCM) (Lipiodol Ultra Fluide®, Guerbet, France) immediately after Hyfosy. The use will be off-label.

Tubal flush with Lipiodol Ultra Fluide® after Hyfosy

Eligibility Criteria

• Age: 18 Years - 40 Years
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Infertile women undergoing Hyfosy as part of the fertility workup. Women will be eligible if they
• are ≥ 18 years and \< 40 years
• have infertility defined as
• lack of conception despite 12 months of unprotected intercourse OR;
• if they are taking part in a donor sperm insemination programme: three cycles of donor insemination without pregnancy OR;
• in case of treated ovulation disorder: three ovulatory ovulation induction cycles without pregnancy
• have tubal patency of at least one Fallopian tube on Hyfosy

You may not qualify if:

• Women with
• known iodine allergy
• allergy to poppy seed oil
• ovulation disorders defined as less than eight menstrual cycles per year who did not have three ovulatory cycles after ovulation induction
• contra-indication to have tubal patency testing according to the site's indication
• active thyroid disorders
• untreated subclinical hypothyroidism (TSH\>2.5mIU/L) in case of auto-immune thyroid disease
• uterine surgery in the past two months before Hyfosy
• a male partner (if applicable)
• with a post-wash Total Motile Sperm Count (TMC) \< 1x106 and/or TMC \< 3x106 in the native sperm analysis \[TMC is defined as volume X concentration X (A\* (progressive) + B\* (non progressive) motility in %) divided by 100\] OR
• with a history suspect of severe male factor infertility if no sperm sample is available at time of randomisation
• an indication for IVF defined as patients who are advised to go to IVF immediately because of bilateral tubal block, severe male factor infertility, unsolved anovulatory problems, endometriosis with residual functional problems"
• no Belgian national number (RRN/INS)
• A+B when A,B,C is used (WHO 2010) A+B+C when A,B,C, D is used (WHO 2021)

Sponsors & Collaborators

• Dafne Balemans: lead

Study Sites (16)

Antwerp University Hospital

Antwerp, Belgium

Location

GZA Sint Augustinus

Antwerp, Belgium

Location

Imelda

Bonheiden, Belgium

Location

AZ Klina

Brasschaat, Belgium

Location

AZ Sint Jan Brugge

Bruges, Belgium

Location

CHIREC

Brussels, Belgium

Location

UCL Saint Luc

Brussels, Belgium

Location

UZ Brussel

Brussels, Belgium

Location

Ziekenhuis Oost Limburg

Genk, Belgium

Location

AZ Sint Lucas

Ghent, Belgium

Location

UZ Gent

Ghent, Belgium

Location

Hôpital Erasme

Lennik, Belgium

Location

UZ Leuven

Leuven, Belgium

Location

CHC Mont Légia

Liège, Belgium

Location

CHR Citadelle

Liège, Belgium

Location

AZ Turnhout

Turnhout, Belgium

Location

Related Publications (1)

• De Neubourg D, Janssens L, Verhaegen I, Smits E, Mol BW, Roelant E. Live birth after additional tubal flushing with oil-based contrast versus no additional flushing: a randomised, multicentre, parallel-group pragmatic trial in infertile women with at least one patent tube at hysterosalpingo-foam sonography (HYFOIL study). BMJ Open. 2021 Nov 29;11(11):e054845. doi: 10.1136/bmjopen-2021-054845.

  PMID: 34845077 DERIVED

MeSH Terms

Conditions

Infertility, Female

Condition Hierarchy (Ancestors)

Genital Diseases, Female; Female Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Genital Diseases; Infertility

Study Design

• Study Type: interventional
• Phase: phase 4
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR INVESTIGATOR
• PI Title: Clinical Trial Center

Study Record Dates

• First Submitted: April 23, 2020
• First Posted: May 8, 2020
• Study Start: May 25, 2021
• Primary Completion (Estimated): June 1, 2027
• Study Completion (Estimated): June 1, 2027
• Last Updated: November 20, 2025

Record last verified: 2025-11

Data Sharing

• IPD Sharing: Will not share

Locations

BE (16)