Post-dural puncture headache (PDPH) is the most common complication of lumbar puncture. Its clinical manifestations are pain in the forehead and the occipital region, or diffuse headache. The pain is dull or fluctuating, becoming worse when standing and better when lying down, and is often accompanied by symptoms including a stiff neck, tinnitus, hearing loss, photophobia, and nausea, which cause great suffering to the patients1. According to epidemiological data, approximately 10% to 30% of the patients who undergo lumbar puncture suffer from PDPH within 48 hours of the procedure.Currently, commonly used treatments for PDPH include rehydration, the administration of corticotropin, caffeine, or sumatriptan, and the application of an epidural blood patch. The efficacy of theophylline has been proven in a placebo-controlled study in which 17 PDPH patients received an intravenous (IV) injection of 200 mg theophylline. The Visual Analogic Scale scores 4 hours after treatment were significantly different compared with those of the placebo group5. At present, the clinical application of theophylline has been replaced by aminophylline and doxofylline, and it is difficult to purchase theophylline in most hospitals in China and other countries. The Aminophylline for Patients With Post-Dural Puncture Headache trial, is a prospective,randomized,double-blind,placebo-controlled trial to evaluate the efficacy and safety of an IV injection of aminophylline on post-dural puncture headache.Eligible patients were randomized in a blinded fashion(1:1) to receive IV injection of aminophyllineor or sterile isotonic saline.The investigators estimate that this trial will demonstrate that an IV injection of aminophylline could be the preferred method for the clinical treatment of PDPH.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
126
Suzhou municipal hospital
Suzhou, Anhui, China
the second hospital of Hebei medcial university
Shijiazhuang, Hebei, China
Henan Province Hospital of Traditional Chinese Medicine
Zhengzhou, Henan, China
Jinzhou central hospital
Jinzhou, Liaoning, China
pain on the Visual Analogue Scale
Time frame: baseline phase
pain on the Visual Analogue Scale
Time frame: 0.5 hour after the Intervention
pain on the Visual Analogue Scale
Time frame: 1 hour after the Intervention
pain on the Visual Analogue Scale
Time frame: 8 hours after the Intervention
pain on the Visual Analogue Scale
Time frame: 1 day after the Intervention
pain on the Visual Analogue Scale
Time frame: 2 days after the Intervention
the overall response to treatment on the Patient Global Impression of Change
Time frame: 2 days after the Intervention
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