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Prophylactic Intrathecal Normal Saline for Prevention of Post Dural Puncture Headache in Women Undergoing Cesarean Section Under Spinal Anesthesia (PDPH)

Primary Purpose

PDPH

Status
Completed
Phase
Phase 4
Locations
Ethiopia
Study Type
Interventional
Intervention
Normal Saline
Sponsored by
Dilla University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for PDPH

Eligibility Criteria

18 Years - 35 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • American society of anesthesiologists' physical status classification(ASA I and II)
  • Term pregnant lady

Exclusion Criteria:

  • patient whose ASA status was greater than three
  • previous history of PDPH
  • previous history of migraine headache
  • BMI greater than 25 kg/m2

Sites / Locations

  • Yassin

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

normal saline

non normal saline

Arm Description

Outcomes

Primary Outcome Measures

incidence of PDPH
occurance of post dural puncture headache
severity of PDPH
severity of PDPH will be assessed with validated scale( visual analog score)

Secondary Outcome Measures

peak sensory block
sensory block
motor block
motor block with bromage score

Full Information

First Posted
May 14, 2020
Last Updated
March 21, 2022
Sponsor
Dilla University
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1. Study Identification

Unique Protocol Identification Number
NCT04393766
Brief Title
Prophylactic Intrathecal Normal Saline for Prevention of Post Dural Puncture Headache in Women Undergoing Cesarean Section Under Spinal Anesthesia
Acronym
PDPH
Official Title
Effectiveness of Prophylactic Intrathecal Normal Saline for Prevention of Post Dural Puncture Headache in Women Undergoing Cesarean Section Under Spinal Anesthesia: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
February 23, 2020 (Actual)
Primary Completion Date
August 23, 2021 (Actual)
Study Completion Date
September 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dilla University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The rates of cesarean section are increasing worldwide despite ten to fifteen percent of World Health Organization recommendation and from which 80-90% of cesarean sections are performed with spinal anesthesia. Post Dural Puncture Headache is the commonest complications associated with spinal anesthesia with prevalence as high as forty percent in Ethiopia. Body of evidence revealed that Conservative managements failed to show significant benefit and epidural needle and catheter techniques didn't provide conclusive evidences. On the other hand, intrathecal injection of normal saline is very safe, simple technique and cost effective in resource limited set up but it is not well examined on its efficacy and safety profiles. The main objective of the study is to assess of efficacy and safety of prophylactic Intrathecal Normal Saline for prevention of Post Dural Puncture Headache in women undergoing cesarean section under spinal anesthesia. After Obtaining Ethical clearance from IRB, a Randomized Controlled Trial study will be conducted in Dilla University Referral Hospital from december2019 to December, 2020. 152 mothers scheduled caesarean section under spinal anesthesia fulfilling the inclusion criteria will be allocated into two groups randomly with random sequence generated list obtained from R package (Random Allocation Rule function) software version 3.6.
Detailed Description
The rates of cesarean section are increasing worldwide despite ten to fifteen percent of World Health Organization recommendation and from which 80-90% of cesarean sections are performed with spinal anesthesia. Post Dural Puncture Headache is the commonest complications associated with spinal anesthesia with prevalence as high as forty percent in Ethiopia. Body of evidence revealed that Conservative managements failed to show significant benefit and epidural needle and catheter techniques didn't provide conclusive evidences. On the other hand, intrathecal injection of normal saline is very safe, simple technique and cost effective in resource limited set up but it is not well examined on its efficacy and safety profiles. The main objective of the study is to assess of efficacy and safety of prophylactic Intrathecal Normal Saline for prevention of Post Dural Puncture Headache in women undergoing cesarean section under spinal anesthesia. After Obtaining Ethical clearance from IRB, a Randomized Controlled Trial study will be conducted in Dilla University Referral Hospital from October 2019 to May, 2020. 152 mothers scheduled caesarean section under spinal anesthesia fulfilling the inclusion criteria will be allocated into two groups randomly with random sequence generated list obtained from R package (Random Allocation Rule function) software version 3.6. Data will be entered, cleaned by Epi-info version 7 and imported to Statistical Package for Social Sciences version 22 for analysis. Descriptive statistics will be run to see the overall distribution of the study subjects with regard to the variables under study. Unpaired student's T-test for continuous symmetric data and Mann Whitney U test for non-normally distributed data will be used to see the mean difference between the groups. Categorical data will be analyzed with Chi square and fisher's exact test where appropriate. Survival analysis will be done to estimate the probability having PDPH within five days postoperatively.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PDPH

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Masking Description
after random generation sequence, the list of 152 were sealed with envelope which later opened by research assistance
Allocation
Randomized
Enrollment
152 (Actual)

8. Arms, Groups, and Interventions

Arm Title
normal saline
Arm Type
Experimental
Arm Title
non normal saline
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Normal Saline
Intervention Description
normal saline(crystalloids)
Primary Outcome Measure Information:
Title
incidence of PDPH
Description
occurance of post dural puncture headache
Time Frame
for five days postoperatively( 12hrs -5 days)
Title
severity of PDPH
Description
severity of PDPH will be assessed with validated scale( visual analog score)
Time Frame
12hrs to 5 days postoperatively
Secondary Outcome Measure Information:
Title
peak sensory block
Description
sensory block
Time Frame
30 minutes after injection of spinal anesthetics
Title
motor block
Description
motor block with bromage score
Time Frame
30 minutes after spinal injection

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: American society of anesthesiologists' physical status classification(ASA I and II) Term pregnant lady Exclusion Criteria: patient whose ASA status was greater than three previous history of PDPH previous history of migraine headache BMI greater than 25 kg/m2
Facility Information:
Facility Name
Yassin
City
Addis Ababa
State/Province
Dilla
ZIP/Postal Code
00419
Country
Ethiopia

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Prophylactic Intrathecal Normal Saline for Prevention of Post Dural Puncture Headache in Women Undergoing Cesarean Section Under Spinal Anesthesia

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