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Clinical trial

Prospective, Single-Center, Randomized, Double-Blind, Clinical Trial for The Evaluation of Pain Associated to The Epidural Tuohy Needle Insertion With Prior Administration of Subcutaneous or Intradermal Lidocaine in Parturient Women Requesting Epidural Analgesia for Laboring Pain.

NCT06236126 is registered in ClinicalTrials.gov with Ohio State University as lead sponsor.

NCT NCT06236126
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Registry record

As filed in ClinicalTrials.gov.

Title
Prospective, Single-Center, Randomized, Double-Blind, Clinical Trial for The Evaluation of Pain Associated to The Epidural Tuohy Needle Insertion With Prior Administration of Subcutaneous or Intradermal Lidocaine in Parturient Women Requesting Epidural Analgesia for Laboring Pain.
Lead sponsor
Ohio State University
Phase
Not applicable
Overall status
Completed
Start date
November 13, 2023
Completion date
January 31, 2026
Enrollment
51 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

analgesia, obstetrical