PROPHYDRA: Role of Prophylaxis by Oral Fluid Supplementation in Prevention of Postdural Puncture Headache

Sponsor
Nantes University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT02859233
Collaborator
(none)
554
4
2
32.4
138.5
4.3

Study Details

Study Description

Brief Summary

Postdural puncture headache (PDPH) is defined, according to the International Headache Society, as any headache develops within 5 days after a lumbar puncture. It worsens within 15 minutes after sitting or standing and improves within 15 minutes after lying.

For preventing PDPH, there are some uncomfortable practices for patients (fluid supplementation and bed rest) and expensive for hospital (time spend for information and management of fluid intake). Patients are usually advised by nurses. If "bed rest" is not effective in prevention of PDPH, "fluid supplementation" is not an advice based on any evidence but only on routine. By this trial, the investigators want to evaluate the scientific value of this advice, in the standard patient care.

The primary objective of this study is to compare oral hyperhydration (2 liters during 2 hours after lumbar puncture - the most common routine according to an internal pilot survey) versus no advice about the fluid intake to prevent the PDPH.

The second objective is to observe the day of apparition of PDPH, between day 0 and day 5.

Condition or Disease Intervention/Treatment Phase
  • Other: Lack of hyperhydration
N/A

Detailed Description

Postdural puncture headache (PDPH) is defined, according to the International Headache Society, as any headache develops within 5 days after a lumbar puncture. It worsens within 15 minutes after sitting or standing and improves within 15 minutes after lying.

For preventing PDPH, there are some uncomfortable practices for patients (fluid supplementation and bed rest) and expensive for hospital (time spend for information and management of fluid intake). Patients are usually advised by nurses. If "bed rest" is not effective in prevention of PDPH, "fluid supplementation" is not an advice based on any evidence but only on routine. By this trial, the investigators want to evaluate the scientific value of this advice by non-inferiority study, in the standard patient care.

The primary objective of this study is to compare oral hyperhydration (2 liters during 2 hours after lumbar puncture - the most common routine according to an internal pilot survey) versus no advice about the fluid intake to prevent the PDPH. It will be evaluated on the occurrence of PDPH in both of the two groups The second objective is to observe the day of apparition of PDPH, between day 0 and day 5.

Study Design

Study Type:
Interventional
Actual Enrollment :
554 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Role of Prophylaxis by Oral Fluid Supplementation in Prevention of Postdural Puncture Headache: A Non-inferiority Randomized Controlled Trial
Actual Study Start Date :
Nov 8, 2016
Actual Primary Completion Date :
Jul 23, 2019
Actual Study Completion Date :
Jul 23, 2019

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control group

Routine advices about the interest of increase fluid after lumbar puncture to prevent PDPH will be transmitted: 2 liters will be provided to be drunk in 2 hours.

Experimental: Interventional group

Lack of hyperhydration : no particular advices will be transmitted about the interest of oral hyperhydration. 500 milliliters will be provided in case of thirst, according to patient's convenience.

Other: Lack of hyperhydration

Outcome Measures

Primary Outcome Measures

  1. The incidence of PDPH. [At D5]

    PDPH will be observed on the 5th day (D5) after the lumbar puncture (D0). If PDPH is still present on the 5th day, the patient continues to be followed until the 8th day after the lumbar puncture

  2. The incidence of PDPH (in case of PDPH still present at D5). [At D8]

    PDPH will be observed also on the 8th day (D8) after the lumbar puncture (D0). , if PDPH was still present on the 5th day, to confirm the diagnosis of PDPH.

Secondary Outcome Measures

  1. The date of apparition of PDPH between day 0 and day 5 [between day 0 and day 5]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient in need of dural puncture for diagnostic.

  • Age between 18 and 60 years old.

  • Patient willing to participate in the research.

Exclusion Criteria:
  • Pregnancy.

  • Contraindication for increased oral fluid intake.

  • Previous dural puncture within 5 day prior enrollment.

  • Parenteral fluid intake superior at 266 ml for 2 hours after dural puncture (1000 ml per day).

  • Enteral artificial feeding.

  • Patient not in capacity to understand correctly French.

  • Patient whose cannot be followed correctly by phone.

  • Patient refusing to participate in the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital centre CHD VENDEE La Roche Sur Yon France 85925
2 Hospital centre LE MANS Le Mans France 72037
3 University Hospital NANTES Nantes France 44093
4 Hospital centre CORNOUAILLE Quimper France 29107

Sponsors and Collaborators

  • Nantes University Hospital

Investigators

  • Principal Investigator: Emmanuelle CARTRON, Nantes University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Nantes University Hospital
ClinicalTrials.gov Identifier:
NCT02859233
Other Study ID Numbers:
  • RC16_0031
First Posted:
Aug 9, 2016
Last Update Posted:
Aug 26, 2019
Last Verified:
Aug 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by Nantes University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 26, 2019