BridgeMD
New treatment option for Postdural Puncture Headache
Official title Effect of Coffee on Postdural Puncture Headache After Cesarean Section
ClinicalTrials.gov ID: NCT07410741
What this study is testing
- What it's testing
- The purpose of this study is to investigate the effects of postoperative coffee consumption on postdural puncture headache (PDPH) and analgesic use in women undergoing cesarean section with spinal anesthesia.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older, women only. Healthy volunteers may be eligible.
You may be able to join if
- Ability to read, understand, and communicate in Turkish
- Age ≥ 18 years
- Undergoing cesarean section under spinal anesthesia
- Spinal anesthesia administered in the sitting position
- Initiation of oral intake at postoperative hour 6
You likely can't join if
- Patients undergoing emergency cesarean section
- Patients with a history of migraine or other types of chronic headache disorders
- Patients in whom spinal anesthesia was converted to general anesthesia.
- Patients whose oral intake was postponed for any reason in the postoperative period.
- Patients with high-risk pregnancies.
- Use of caffeine-containing analgesic medications during the postoperative period.
See the full eligibility criteria
- Ability to read, understand, and communicate in Turkish
- Age ≥ 18 years
- Undergoing cesarean section under spinal anesthesia
- Spinal anesthesia administered in the sitting position
- Initiation of oral intake at postoperative hour 6
- No history of physiological discomfort related to coffee consumption based on prior experience (e.g., insomnia, palpitations, headache)
- Ability to understand the study procedures and communicate adequately to provide informed consent
- Patients undergoing emergency cesarean section
- Patients with a history of migraine or other types of chronic headache disorders
- Patients in whom spinal anesthesia was converted to general anesthesia.
- Patients whose oral intake was postponed for any reason in the postoperative period.
- Patients with high-risk pregnancies.
- Use of caffeine-containing analgesic medications during the postoperative period.
- Postoperative cigarette smoking.
The study team makes the final eligibility decision.
Where it's taking place
- Ankara, Ankara, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Ankara, Ankara, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.