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NCT03045939: DoubleCRIB
Cervical Ripening With the Double Balloon Device for 6 Hours Compared With 12 Hours
NA trial testing cervical ripening device in Induction of Labor in 200 participants. Status unknown.
1 February 2019
Quick facts
| Lead sponsor | Bnai Zion Medical Center |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | other |
| Enrollment | 200 |
| Start date | 1 March 2017 |
| Primary completion | 1 February 2019 |
| Estimated completion | 1 March 2019 |
| Sites | 1 location across Israel |
Drugs / interventions tested
- cervical ripening device
Conditions studied
- Induction of Labor — all drugs for Induction of Labor →
- Unfavorable Cervix — all drugs for Unfavorable Cervix →
Sponsor
Bnai Zion Medical Center
Who can join
18 and older, female only, with Induction of Labor or Unfavorable Cervix. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study will evaluate the insertion of double balloon device (DBD) for cervical ripening for 12 h vs 6 hours.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Double-Balloon Device for 6 Compared With 12 Hours for Cervical Ripening: A Randomized Controlled Trial.
Bleicher I, Dikopoltsev E, Kadour-Ferro E, Sammour R, et al · · 2020 · cited 20× · PMID 32282603 · DOI 10.1097/aog.0000000000003804 -
Cervical ripening with a double balloon device for 6 h in patients with a long cervix: Secondary analysis of a randomized controlled trial.
Sammour R, Dikopoltsev E, Sagi S, Vitner D, et al · · 2025 · PMID 39445570 · DOI 10.1002/ijgo.15955
Verify or expand the search:
- PubMed search for NCT03045939
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Induction of Labor
Currently open trials in the same condition.
- NCT06803992 — Induction of Labor - Comparison Propess With Prostaglandin E2 Vaginal Gel and Balloon Catheter · Phase 4 · recruiting
Other Bnai Zion Medical Center trials
Trials by the same sponsor.
- NCT07323901 — GRAPE-GDM Prospective Comperative Trial - Grape Juice as a Replacement Drink for Gestational Diabetes Screening · NA · enrolling by invitation
- NCT06487169 — Effectivity Gas Extraction to Prevent Anesthesiologists Waste Gas Exposure of Sevofluorane During Pediatric Induction · not yet recruiting
- NCT06581185 — Pseudotumor Cerebri Headache Ten Years Outcome · enrolling by invitation
- NCT07288021 — Topical Anesthesia During Catheter Insertion for Cervical Ripening (TOLERANCE) · Phase 4 · recruiting
- NCT06190964 — Integrative Medicine for Hospital Workers Exposed to War · NA · unknown
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03045939 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Bnai Zion Medical Center
- Last refreshed: 5 March 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03045939.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing