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CompletedNCT04933500Updated Dec 15, 2022

Regional Anesthesia

An observational study in Anesthetic Regional Techniques for Vaginal Surgeries, sponsored by Reham Ali Abdelhaleem Abdelrahman. Completed at 1 site in Egypt. Open to female participants aged 25 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-12-15.

Sponsored by Reham Ali Abdelhaleem Abdelrahman · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
88
Ages
25 Years to 55 Years
Sex
Female
01

Study summary

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

02

Conditions studied

  • Anesthetic Regional Techniques for Vaginal Surgeries
03

In context

Lead sponsor

Reham Ali Abdelhaleem Abdelrahman is the lead sponsor of 6 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 55 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

adult female Egyptian patients

Inclusion criteria

  • ASA I-II

    --Age(25-55)years

  • Height(150-170cm)

Exclusion criteria

Exclusion Criteria:

  • patient refusal
  • severe mitral or aortic stenosis
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
88 participants (actual)
Target follow-up
6 Months
Patient registry
Yes

Groups and cohorts

  • Conventional epidural

    epidural needle: Tuhoy needle 1.3mm (18 G) with 20G multi-orifice epidural catheter

  • Dural puncture epidural

    epidural needle;Tuhoy needle 1.3mm (18G)with 20G multi-orifice epidural catheter and 25G Whitacre spinal needle

    Device: Whitacre spinal needle

Interventions

  • DeviceWhitacre spinal needle

    25G Whitacre spinal needle

06

What researchers measure

Primary outcomes

  1. Onset of bilateral sacral sensory loss

    sacral sensory loss is observed by needle brick

    Time frame: 4months

07

Study locations

1 site
  • Abdelrahman
    Cairo, 11562, Egypt
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 15, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04933500
Lead sponsor
Reham Ali Abdelhaleem Abdelrahman
Responsible party
Reham Ali Abdelhaleem Abdelrahman (Anesthesia lecturer M.D., Cairo University) — Sponsor-investigator
First posted
Jun 21, 2021
Start date
Jul 1, 2021
Primary completion
Oct 1, 2022
Completion
Dec 1, 2022
Last update
Dec 15, 2022

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2022. You cannot join it, but the record below documents what was studied.

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