Clinical TrialID 8394

The Effect of IV PAPAVERINE 80 mg Prior to Catheter Balloon Insertion on Bishop Score and Pain

NCT05759364

Induction of Labor|Pain, Acute|Labor Pain|Delivery Delayed

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Record Fields

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Clinical Trial Id
8394
Evidence Id
8394
Core Evidence Id
8394
Source Clinical Trial Id
8392
Herb2 Clinical Trial Id
HBCT008392
Nct Id
NCT05759364
Title
The Effect of IV PAPAVERINE 80 mg Prior to Catheter Balloon Insertion on Bishop Score and Pain
Status
Recruiting
Phase
Study Result
No
Study Condition
Induction of Labor|Pain, Acute|Labor Pain|Delivery Delayed
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: TRIPLE (PARTICIPANT, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Intervention
DRUG: IV Papaverine 80 mg|DRUG: Placebo
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Triple
Intervention Purpose
Treatment
Gender
Female
Age
Adult
Enrollment
128
Outcome Measure
The delta Bishop score, The difference between the bishop score (a score of the cervix ripening) before and after the insertion of Foley catheter. Higher delta Bishop scores means better outcome, 1 year|Pain during insertion of the catheter, Pain during insertion of the catheter based on visual scale analoug (0-10) score, . The minimum is 0, the maximum is 10. Higher score means worse outcome, 1 year
Sponsor Collaborator
Western Galilee Hospital-Nahariya
Funded By
OTHER_GOV
Location
Galilee Medical Center, Nahariya, Hazafon, Israel
Other Id
0012-23-NHR
Start Date
2023-05-15
Primary Completion Date
2024-04-01
Completion Date
2025-04-01
First Posted
2023-03-08
Results First Posted
Last Update Posted
2023-06-29
Study Document
Study Url
https://clinicaltrials.gov/study/NCT05759364
Title Cn
Title En
The Effect of IV PAPAVERINE 80 mg Prior to Catheter Balloon Insertion on Bishop Score and Pain
Bilingual Status
semi_complete