Clinical Trial Search

Primary: Participants Who Report Post Dural Puncture Headaches — 21; 27 Participants — p=.877

Primary: Number of Patients (in Digits) Got Earlier Relief of PDPH (in Hours) After Use of Hydrocortisone or Mannitol. — 25; 25 Participants

Primary: Number of Participants With Postdural Puncture Headache — 3; 4; 8; 10 Participants

Primary: Postdural Puncture Headache in Patients Receiving Spinal Anesthesia for Cesarean Section — 14; 10 participants

Primary: Headache Pain Score — 6.67; 2.33 units on a scale

Primary: Frequency of Moderate or Severe Headache After Emergency Department (ED) Discharge — 31; 29; 42; 44 Participants — p=0.751

Primary: Number of Participants With Sustained Headache Relief — 12 Participants

Primary: 0-10 Pain Scale on Which 0 = no Pain and 10= the Worst Pain Imaginable — 5.2; 3.8 units on a scale

Primary: Number of Participants Who Required Asymmetric Block, Top-up Interventions, Catheter Adjustments, Replacement of Epidural Catheter, or Failure of Block Requiring…

Primary: Onset Time of Surgical Anesthesia — 422; 655 seconds

Primary: Frequency of Postoperative Headache in Elective Surgery Patients — 126; 37; 89 participants

Primary: Persistent Pain-PERCEIVED STRESS Scores Stratified by the Rate of Recovery — 11.4; 12.9; 15.4 units on a scale — p=<0.01

Primary: Epidural Pressure Sensitivity at Level of Epidural Insertion — 26.8; 26.8; 47.6 force (newtons/cm^2)

Primary: Number of Participants Who Report Moderate or Severe Pain Within 24 Hours of Emergency Department(ED) Discharge — 53; 6; 20 Participants

Primary: DB Period: Mean Change From Baseline in Monthly Average Number of Headache Days of at Least Moderate Severity During the 12-Week Treatment Period After the First Dose of…

Primary: Number of Participants With Adequate Relief of Headache as a Measure of Efficacy — 34; 32 Participants — p=0.14

Primary: Number of Participants With Response to Occipital Nerve Block in Pregnancy — 20; 16 Participants — p=0.30

Primary: Post Operative Fentanyl PCA Consumption — 300; 446 µg

Primary: Change in Optic Nerve Sheath Diameter by Ultrasonography — 0.02; 0.02 mm — p=0.98

Primary: Reduction in Pain Scores at 60 Minutes — 48.7; 48.3 reduction in visual analog pain score

Primary: NRS Score for Pain (0-10) With Movement 24 Hours After Spinal Administration — 4; 3 score on a scale — p=0.132

Primary: Incidence of Post-operative Nausea and/or Vomiting — 29; 24 Participants

Primary: The Primary Outcome Will be Pain Relief Sufficient for Discharge From the Emergency Department. — 16; 14; 2 Participants

Primary: Change in Headache Relief — 23 percentage of headaches resolved — p=.079

Primary: Persistent Headache Pain Free at 24 Hours — 26; 19 Participants

Primary: Intracranial Pressure Measurements Estimated by the MRICP Technique. — 6.5 cm H20

Primary: Pain Score, Visual Analogue Pain Scores — 1.9 units on a scale

Primary: Pain Intensity — 5.82; 4.92 score on a scale

Primary: Number of Participants With Sustained Headache Relief Assessed by Self-evaluation — 20; 37 Participants

Primary: Incidence of New-onset Category II or III Fetal Heart Rate Tracings — 72; 52 Participants