Multimodal Approach to the Intrathecal Catheter for Obstetric Accidental Dural Puncture

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

39 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-03-01

Study Completion Date

2023-02-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Accidental dural puncture is an uncommon complication of epidural analgesia and can cause postdural puncture headache.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Post-dural Puncture Headache: A Retrospective Study

NCT03790124

Obstetric Anesthesia Problems Headache Epidural; Anesthesia, Headache

COMPLETED

Chronic Headache and Chronic Backache Following Unintentional Dural Puncture at Delivery Room.

NCT03908424

Parturient Who Underwent Epidural Anesthesia During Which an Unintentional Dural Punctur Occurred Parturient Who Develop a Postdural Puncture Headache Parturient Who Gave Informed Consent to Participation in the Study

COMPLETED

Alteration in Hearing Following Accidental Dural Puncture. A Study in Parturients

NCT01682967

Parturients in Labour

COMPLETED

The Occurrence of Post Dural Puncture Headache After Epidural Blood Patch

NCT03080610

Post-Dural Puncture Headache

COMPLETED

Incidence of Headache Following an Unintentional Dural Puncture

NCT01977898

Postdural Puncture Headache Post-Lumbar Puncture Headache Cerebrospinal Fluid Leaks

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The aim of this study the effectiveness of a protocol implemented in our department, according to the recommendations of good practice, on the reduction of the use of blood patchs in patients who have had an accidental dural puncture during the implementation of their spinal anesthesia, in order to prevent the use of the blood patch. In addition, intensity of headaches is evaluated.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Spinal Anesthetics Causing Adverse Effects in Therapeutic Use

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

patients having an accidental dural puncture during the installation of an epidural anesthesia

patients having an accidental dural puncture during the installation of an epidural anesthesia will be included.

Analysis datas of medical record.

collection of data from the medical record

Intervention Type OTHER

collection of data from the medical record:

1. During epidural space puncture = cerebrospinal fluid (CSF) reflux, presence of glucose / strip, saline injection, intrathecal catheter insertion, intrathecal levobupivacaine and sufentanil injection, catheter insertion time, number of punctures, function of the person performing the procedure.
2. Analgesia and hemodynamics during labor, blood pressure, pulse rate, amount of local anesthetic used, whether emergency cesarean section was performed
3. Demographic data (age, weight, height, body mass index (BMI))
4. Post-partum monitoring of decubitus or orthostatic headaches, intensity, any other associated clinical signs
5. Analgesics used and their efficacy
6. The use of one or more blood patches, with the volume injected and their efficacy
7. Identification of the breach during epidural analgesia or after delivery
8. Call the patient at 1 week to reassess the episode and its consequences.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

collection of data from the medical record

collection of data from the medical record:

1. During epidural space puncture = cerebrospinal fluid (CSF) reflux, presence of glucose / strip, saline injection, intrathecal catheter insertion, intrathecal levobupivacaine and sufentanil injection, catheter insertion time, number of punctures, function of the person performing the procedure.
2. Analgesia and hemodynamics during labor, blood pressure, pulse rate, amount of local anesthetic used, whether emergency cesarean section was performed
3. Demographic data (age, weight, height, body mass index (BMI))
4. Post-partum monitoring of decubitus or orthostatic headaches, intensity, any other associated clinical signs
5. Analgesics used and their efficacy
6. The use of one or more blood patches, with the volume injected and their efficacy
7. Identification of the breach during epidural analgesia or after delivery
8. Call the patient at 1 week to reassess the episode and its consequences.

Intervention Type OTHER