Skip to content

Effect of Epidural Needle Injection on Catheter Placement Success During Painless Labour

Effect of Epidural Needle Injection on Catheter Placement Success During Painless Labour: A Prospective Randomized Study

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07327918
Enrollment
216
Registered
2026-01-08
Start date
2026-06-28
Completion date
2027-02-15
Last updated
2026-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Labour Analgesia

Keywords

Epidural Needle

Brief summary

Epidural analgesia is the gold standard for painless labour, but successful catheter placement can be technically challenging due to anatomical and physiological changes in pregnancy. Injecting saline or local anesthetic through the epidural needle before catheter insertion has been proposed to facilitate catheter advancement by dilating the epidural space. This study aimed to evaluate the effect of epidural needle injection on the success rate and ease of catheter placement during labour analgesia.

Interventions

Patients will receive \[10 ml of local anesthetic\] through an epidural needle before catheter advancement.

OTHERControl group

No injection before catheter insertion.

Sponsors

Benha University
CollaboratorOTHER
Al-Azhar University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Female patients aged 18-40 years. * ASA physical status II or III. * Singleton pregnancy. * Gestational age ≥37 weeks. * Active labour with cervical dilatation ≥3 cm. * Cephalic presentation. * Requesting epidural analgesia for painless labour. * Ability to provide written informed consent.

Exclusion criteria

* • Refusal to participate or to sign informed consent. * Age \<18 or \>40 years. * ASA status ≥IV. * Allergy to local anesthetics or saline. * Coagulopathy or platelet count \<100,000/mm³. * Local infection at the insertion site. * Severe spinal deformity (scoliosis, kyphosis). * Multiple pregnancy. * Non-cephalic presentation (breech, transverse). * Antepartum hemorrhage or placenta previa. * Severe preeclampsia or eclampsia. * Signs of fetal distress. * Previous lumbar spine surgery. * Difficult epidural anatomy (on ultrasound or palpation). * BMI \>40 kg/m²

Design outcomes

Primary

MeasureTime frameDescription
Success of epidural catheterization on the first attempt.Assessed immediately during the procedure at the time of epidural catheter placement.The incidence of success of epidural catheterization on the first attempt will be determined. This measures whether the epidural catheter is successfully inserted on the first attempt after loss of resistance, without the need for repositioning or reattempt. Success is defined by obtaining adequate analgesia with proper catheter function (confirmed by clinical effect).

Secondary

MeasureTime frameDescription
Number of catheterization attemptsAssessed during the procedure until successful catheterization is achieved.Counts the total number of insertion attempts required to achieve correct epidural catheter placement, reflecting technical ease and procedural efficiency.
Procedure durationAssessed intraoperatively, recorded from the beginning of the puncture until catheter fixation.Measures the time elapsed between needle insertion and successful catheter placement, expressed in minutes. Shorter duration indicates greater ease of insertion.
Incidence of numbnessAssessed post-catheter insertion, within the first 30 minutes after drug administration.Records any occurrence of unexpected or abnormal sensory numbness following the epidural test dose or analgesic administration, which may indicate uneven drug spread or misplaced catheter.
Incidence of unintended dural punctureAssessed immediately at the time of needle insertion or catheter placement.Identifies accidental dural puncture events occurring during epidural space entry or catheter advancement.
Maternal satisfactionAssessed post-delivery, usually within 24 hours after labour.Evaluates the mother's satisfaction regarding the analgesia quality, comfort during the procedure, and overall experience. Typically rated using a structured satisfaction scale. Maternal satisfaction can be measured on a 0-5 scale using a simple 5-point Likert-type item: 0 = completely dissatisfied, 1 = dissatisfied, 2 = neutral, 3 = satisfied, and 4 = very satisfied.

Countries

Egypt

Contacts

Primary ContactNeveen A Kohaf, Ph.D
nevenabdo@azhar.edu.eg+201060383012

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026