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Adverse Effect clinical trials

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NCT ID: NCT02854787 Completed - Hypotension Clinical Trials

Intravenous Bolus of Phenylephrine vs. Norepinephrine in Preventing Hypotension After Spinal Anesthesia

NorPN
Start date: May 2016
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determine if an intravenous bolus of phenylephrine is more effective compared to an intravenous bolus of norepinephrine associated with crystalloid loading for maintaining blood pressure during a spinal anesthetic for a cesarean delivery. Prevention of low blood pressure has been shown to decrease nausea and vomiting during and after cesarean delivery under spinal anesthesia. For elective cesarean delivery, all participants will receive spinal anesthesia with a local anesthetic and sufentanil. This study plans to enroll 120 pregnant women. Patients will be randomly assigned according to a computer generated system to be in one of two groups.

NCT ID: NCT02768168 Completed - Adverse Effect Clinical Trials

The Effects of Dezocine Pretreatment on Dexamethasone Induced Perineal Irritation

Start date: May 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the efficacy of dezocine pretreatment on dexamethasone 21-phosphate induced perineal irritation (include pian and pruritus).

NCT ID: NCT02709824 Completed - Adverse Effect Clinical Trials

Anti-staining Efficacy of Anti-Discoloration System (ADS) Added to Chlorhexidine (CHX)

CHX+ADS
Start date: December 2011
Phase: N/A
Study type: Interventional

Dental staining is the most common local side effect of chlorhexidine (CHX) mouthwashes. A prospective, cross-over, randomized clinical trial will be carried out in triple blind to compare the effect on dental staining of two 0.12% CHX mouthwashes: with or without ADS. Twenty-two healthy subjects will be enrolled. Briefly, the study includes two sequential stages: in the first phase, we record the "immediate" objective and subjective evaluation of dental discoloration by spectroscopic and questionnaire-based analyses, at baselines and after each 21 days long-cycle of mouthwash. A wash-out period between the cycles of 21 days is performed. In the second phase, a long-term (after 6 months) subjective evaluation of dental discoloration was obtained by means of clinical photograph visual analysis and new questionnaires.