Houston, TX 的 偏頭痛 臨床試驗
7 項針對 偏頭痛 的研究正在 Houston(約 30 英里範圍內)及其周邊地點尋找參與者。開啟研究以查看參與資格及聯絡研究團隊的方式。
官方研究文本(英文)
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Study of EVO756 in Adults With Migraine
招募中2 期
- SFF Medical Research Group LLC, Houston
- Mercury Clinical Research Inc. - Houston Neurology Associates, Houston
Efficacy and Safety Study of Rimegepant for the Preventative Treatment of Migraine in Pediatric Subjects
招募中3 期
- DM Clinical Research - Cy Fair, Houston
- SCLA Management - Drop Box, Houston
- SCLA Management Office, Houston
- 還有 1 項
Long-term Safety Study of Rimegepant in Pediatric Subjects for the Acute Treatment of Migraine
招募中3 期
- Pain and Headache Centers of Texas, Houston
- SCLA Management, Houston
- NeuroCare Plus, Houston
- 還有 1 項
Randomized Study in Children and Adolescents With Migraine: Acute Treatment
招募中3 期
- UTHealth Houston, Houston
- Pain and Headache Centers of Texas, Houston
- SCLA Management, Houston
- 還有 2 項
A Study of Oral Atogepant Tablets to Assess Adverse Events and Change in Disease Activity To Prevent Migraine in Participants Aged 12 to 17 Years
招募中3 期
- Earle Research /ID# 270424, Houston
Study to Assess Adverse Events and Disease Activity of Oral Ubrogepant Tablets for the Acute Treatment of Migraine in Children and Adolescents (Ages 6-17)
招募中3 期
- DM Clinical Research /ID# 229826, Houston
- Aavon Clinical Trials /ID# 279007, Houston
- Houston Clinical Research Associates /ID# 244889, Houston
- 還有 1 項
A Study to Evaluate the Efficacy and Safety of Elismetrep (K-304) in the Acute Treatment of Migraine
招募中3 期
- Victorium Clinical Research, Houston
- DM Clinical Research, Houston
其他城市的 偏頭痛 試驗
- Cincinnati, OH11 項研究
- Miami, FL8 項研究
- Austin, TX8 項研究
- Philadelphia, PA8 項研究
- Concord, CA8 項研究
- Amherst, NY7 項研究
- Omaha, NE7 項研究
- Washington, DC7 項研究
- Aurora, CO6 項研究
- Stamford, CT6 項研究
- San Diego, CA6 項研究
- Tampa, FL6 項研究
Houston 的其他研究
- 非小細胞肺癌145 項研究
- 乳癌126 項研究
- 癌症(所有類型)121 項研究
- 轉移性癌症104 項研究
- 大腸直腸癌102 項研究
- 卵巢癌89 項研究
- 急性髓系白血病85 項研究
- 肺癌78 項研究
- 前列腺癌76 項研究
- 子宮內膜癌68 項研究
- 胰臟癌61 項研究
- 黑色素瘤59 項研究
資料來源:ClinicalTrials.gov,擷取日期 2026年10月5日。各研究自行設定資格標準;由研究團隊決定參與者資格。