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Headache clinical trials

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NCT ID: NCT03967483 Not yet recruiting - Headache, Migraine Clinical Trials

Study on Indomethacin-responsive Headaches

Start date: June 1, 2019
Phase:
Study type: Observational

Description of modalities concerning the patient care of headaches sensible to indometacine.

NCT ID: NCT03966547 Withdrawn - Clinical trials for Postdural Puncture Headache

Changes in Cerebral Blood Flow (CBF) in Prone and Sitting Position Before and After GSP-block and Before and After Epidural Blood-patch: A Substudy of NCT03652714

Start date: May 2020
Phase: N/A
Study type: Interventional

The purpose of this optional sub-study to GSPB-2018 (NCT03652714) is to evaluate the changes in cerebral blood flow (CBF) under different conditions to understand if postdural puncture headache is caused by changes in the cerebral blood flow and if treatment normalises that change.

NCT ID: NCT03960749 Completed - Clinical trials for Post-Lumbar Puncture Headache

Headache After Diagnostic Lumbar Puncture

HELPUmeå
Start date: May 28, 2013
Phase: N/A
Study type: Interventional

The objectives of this study are to investigate the effects of needle design, needle size and stylet reinsertion on the risk for headache after diagnostic LP (lumbar puncture, Post-LP headache). The following needles are used in the study: 1. Sprotte 25 Gauge (G) (0.5 mm) atraumatic needle with introducer 2. Sprotte 22 G (0.7 mm) atraumatic needle with introducer 3. Spinocan 25 G (0.5 mm) cutting needle

NCT ID: NCT03951649 Completed - Pregnancy Related Clinical Trials

Acute Headache Treatment in Pregnancy: Occipital Nerve Block vs PO Acetaminophen With Caffeine

Start date: February 10, 2020
Phase: Phase 4
Study type: Interventional

This is an open label randomized controlled trial evaluating response to bupivacaine occipital nerve block compared to Tylenol/Caffeine cocktail in treatment of pregnant patients seeking care of headache.

NCT ID: NCT03944876 Recruiting - Cluster Headache Clinical Trials

Botulinum Toxin Type A Blockade of the Sphenopalatine Ganglion in Treatment-refractory Chronic Cluster Headache

BASIC
Start date: November 1, 2019
Phase: Phase 3
Study type: Interventional

Cluster headache is a primary headache condition characterized by clusters of one-sided, high-intensity pain attacks. The headache may be episodic or chronic. Treatment options are limited and their effects unsatisfactory. An important nerve pathway involved in the pain attacks has a switching station at the sphenopalatine ganglion (SPG) located in the depth of the facial bones. SPG is a known therapy target for cluster headache. The area can be identified on CT images, but is difficult to access due to its location. Thus, the Multiguide navigation system has been developed to enable precise delivery of the drugs that target SPG activity. In Trondheim, two phase 1 / Phase 2 study have been carried out using botulinum toxin A (Botox®) against SPG in patient with chronic cluster headache and chronic migraine. The results indicate that such a treatment strategy is safe and beneficial. The current study is a randomized, placebo-controlled, triple-blinded study to investigate whether precise single-injection of botulinum toxin A reduces the frequency of attacks in chronic cluster headache .

NCT ID: NCT03928496 Completed - Clinical trials for Post-Traumatic Headache

Abobotulinumtoxina Efficacy in Post-Traumatic Headache

Start date: August 1, 2013
Phase: Phase 4
Study type: Interventional

This study will evaluate the efficacy of abobotulinumtoxina on Veterans with post-traumatic headache

NCT ID: NCT03919630 Completed - Clinical trials for Cervicogenic Headache

Mobilization Versus Manipulation for the Treatment of Cervicogenic Headaches

Start date: May 1, 2019
Phase: N/A
Study type: Interventional

There is currently a gap within the literature as to the effects of a thrust versus non-thrust mobilizations techniques specifically to the upper cervical spine C0-C3 along with home exercise program to help reduce frequency and intensity of cervicogenic headaches. Therefore, the purpose of this study is to examine the effectiveness of in treating headaches using non-thrust or thrust mobilizations in addition to postural corrective exercises on patient outcomes measures.

NCT ID: NCT03915639 Not yet recruiting - Pain, Postoperative Clinical Trials

Effect of the Peri-incisional Multimodal Cocktail Infiltration on Postcraniotomy Headache

Start date: April 2022
Phase: N/A
Study type: Interventional

Postcraniotomy headache (PCH) has been underestimated for the past decades. However, current treatments for PCH are either considered insufficient or accompanied by severe side-effects. Some studies revealed that peri-incisional injection of a mixed cocktail that contains ropivacaine, epinephrine, ketorolac, and methylprednisolone showed significant efficacy in relieving postoperative pain after total hip or knee arthroplasty. Previous literature reported that the cause of PCH was related to incision of the scalp and dura, which is considered similar to causes to postoperative pain after total hip or knee arthroplasty. Thus, investigators suppose that the cocktail mixture can better relieve PCH in adults.

NCT ID: NCT03910088 Completed - Clinical trials for Post-Dural Puncture Headache

Pregabalin Versus Hydrocortisone for Postdural Puncture Headache After Spinal for Cesarean

PDPH
Start date: April 20, 2019
Phase: Phase 4
Study type: Interventional

Postdural puncture headache (PDPH) is a common complication after spinal anesthesia. The role of pregabalin and hydrocortisone in the treatment of PDPH is unclear. The aim of this work is to assess and compare the efficacy of both drugs in severe cases of PDPH after spinal anesthesia for elective cesarean section.

NCT ID: NCT03908944 Withdrawn - Postoperative Pain Clinical Trials

Postoperative Pain and Headache After Craniotomy

Start date: January 2, 2019
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the outcomes of an anesthetic technique which is not synthetic opioid based, on postoperative pain modulation and development of post craniotomy headache against a cohort of patients where an opioid based standard anesthetic technique was used for craniotomy. The hypothesis that is tested is that the use of agents other than synthetic short acting opioids will reduce the amount of postoperative pain and the incidence of headache after surgery.