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Dural Puncture Epidural Technique Versus Conventional Epidural Technique During Vaginal Surgeries

N

National Research Centre, Egypt

Status

Withdrawn

Conditions

Dural Puncture Epidural Technique

Treatments

Procedure: Dural puncture epidural
Procedure: Conventional epidural

Study type

Interventional

Funder types

Other

Identifiers

NCT04921761
Dural Puncture

Details and patient eligibility

About

The study aims to evaluate whether the dural puncture epidural technique (group B) improves sacral block anesthesia during vaginal surgeries compared with the conventional epidural technique (group A).

Sex

Female

Ages

25 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Age (25- 55) years. Height (150 -170) cm.

Exclusion criteria

Patient refusal. Hypersensitivity to local anesthetic drugs. Bleeding disorders and coagulopathy. Severe mitral or aortic stenosis. Local or systemic sepsis. Uncooperative patients. Sever spinal deformity. Blood or CSF in the epidural catheter during the procedure. Failure of the block and need for general anesthesia.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

0 participants in 2 patient groups, including a placebo group

Group A
Placebo Comparator group
Description:
Women who received the conventional epidural technique (group A). Intervention: Procedure: Conventional epidural
Treatment:
Procedure: Conventional epidural
Group B
Active Comparator group
Description:
Women who received the dural puncture epidural technique (group B). Intervention: Procedure: Dural puncture epidural
Treatment:
Procedure: Dural puncture epidural

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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