110
Participants
Start Date
August 12, 2024
Primary Completion Date
March 23, 2025
Study Completion Date
March 23, 2025
Papaverine
Within 30-minutes prior to catheter insertion, women in the intervention group will receive IV-papaverine 80 mg in 100 ml 0.9% saline
placebo
I.V Sallne
Galilee Medical Center, Nahariya
Western Galilee Hospital-Nahariya
OTHER_GOV