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OpenTrials
Completed

NCT Number: NCT04933500

Regional Anesthesia

Both techniques are efficacious for sacral anesthesia during vaginal surgeries. Dural puncture epidural technique allows partial confirmation of epidural catheter placement.

Completed

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Key information

Age range

25 year–55 year

Sex eligibility

Female

Study type

Observational

Primary location

Abdelrahman

Cairo, 11562, Egypt

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ASA I-II

--Age(25-55)years

  • Height(150-170cm)

Exclusion criteria

  • patient refusal
  • severe mitral or aortic stenosis

Treatment and study plan

Whitacre spinal needle

Device

25G Whitacre spinal needle

Primary outcomes

  1. Onset of bilateral sacral sensory loss

    Time frame: 4months

    sacral sensory loss is observed by needle brick

Sponsors and collaborators

Lead sponsor

Reham Ali Abdelhaleem Abdelrahman

Other

Registry information

Official study title

Comparative Study Between Dural Puncture Epidural Technique and Conventional Epidural Technique During Elective Gynecological Vaginal Surgeries

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Jun 21, 2021
Registry last updated
Dec 15, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.