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NCT ID: NCT04824456 Enrolling by invitation - Clinical trials for to Assess Neurosensory Function of Inferior Alveolar Nerve After BSSO

Neurosensory Assesment After Using Separators Vs Chisels in Bilateral Sagittal Split Mandibular Osteotomy. RCT

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

The bilateral sagittal split Ramus osteotomy (BSSRO) was introduced by Trauner and Obwegeser. Since then, many modifications of this procedure have been reported, leading to a less difficult and more predictable procedure for correcting mandibular anomalies. persistent post-operative neurosensory disturbances of the inferior alveolar nerve are still one of the major complications of this operation. The incidence has decreased over the years due to improved techniques and the use of different instruments. However, most recent series still report postoperative persistent hypesthesia of the inferior alveolar nerve in more than 10% of the patients up to 48%. There are no reports on the influence of other surgical variables on the persisting post-operative hypesthesia. Several methods have been reported for evaluating neurosensory disturbances of the inferior alveolar nerve. One of the simplest methods reported is tactile evaluation based on subjective sensation reported by the patients. Many authors have used this method in their evaluation of post-operative hypesthesia.

NCT ID: NCT05184179 Enrolling by invitation - Hypertension Clinical Trials

Observational Study to Evaluate the Therapeutic Effectiveness and Safety of Olomax Tab

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

Throughout this study, the efficacy and safety information of Olomax tablets will be collected from 24 weeks to 48 weeks(+8 weeks) The Data collection point is baseline, at more than 24 weeks, at more than 48 weeks(+8 weeks).

NCT ID: NCT05433948 Enrolling by invitation - Liver Cirrhosis Clinical Trials

Diagnosing Minimal Hepatic Encephalopathy

MindTheLiver
Start date: December 1, 2019
Phase:
Study type: Observational

Our purpose is to 1. Examine the correlation between MDF in a resting EEG, recorded just before the CRT test, and the variance in reaction times indicated by the CRT index 2. At simultaneous CRT and EEG recording, examine whether a change in EEG is seen immediately before an extended reaction time occurs (defined by the 75th percentile). This will shed light on a direct pathophysiological association between what is measured with EEG and CRT. 3. Investigate whether cyclicity can be detected in the continuous reaction times and if so, whether amplitude and wavelength in this cyclic activity are correlated to EEG parameters. 4. Examine whether a response to standard HE treatment can be detected with EEG in patients who are thought to suffer from it. As well as if baseline outcome predict future hepatic encephalopathy. 5. With a view to further validating our findings, investigators want to correlate results from EEG and CRT with the most internationally widespread psychometric test, the Portosystemic Encephalopathy test (PSE), which necessitates the establishment of Danish normal values. A secondary purpose of this study is therefore 6. To establish Danish normal values for the PSE test and the Animal Naming test in Danes

NCT ID: NCT04237844 Enrolling by invitation - Clinical trials for Bronchopulmonary Dysplasia

Clinic Features and Outcome of BPD (SGBPD)

Start date: December 1, 2020
Phase:
Study type: Observational

This study described the perinatal high-risk factors and clinical manifestations of the children, and compared the high-risk factors, clinical manifestations and prognosis of BPD among different clinical subtypes by comparison between groups. BPD grading was performed using the 2018 grading standard to compare the distribution of I/II/III BPD among different groups.

NCT ID: NCT04290078 Enrolling by invitation - Low Back Pain Clinical Trials

The Kaia Back Pain Intervention for Self-management of Low Back Pain

BACKSPIN
Start date: December 1, 2020
Phase: N/A
Study type: Interventional

The study aims to evaluate outcomes of the use of Kaia Study app (software program application for self-management of low-back pain) on back pain among adults with non-specific subacute and chronic low back pain based on change in pain intensity, physical functioning, quality of life (PROMIS-10) based on self-reported information from baseline to study end as compared to a control group.

NCT ID: NCT04350268 Enrolling by invitation - Adults Clinical Trials

Adult Social Interaction

Start date: December 1, 2020
Phase:
Study type: Observational

This study will collect vocalization data from healthy adults during regular daily activity.

NCT ID: NCT04371445 Enrolling by invitation - Post-operative Pain Clinical Trials

Dextenza in the Post-op Management of Vitreoretinal Surgeries

Start date: December 1, 2020
Phase: Phase 4
Study type: Interventional

This study will assess the control of inflammation at days 1, 7, 14, and 21 days following the vitreoretinal surgical procedure analyzing two randomized study arms: Intracanalicular dexamethasone insert group or topical steroid drop group. Patients must be 18 years of age and older, of any race and either sex, requiring surgery with the procedure type of pars plana vitrectomy for either the indication of macular hole, epiretinal membrane removal, or vitreomacular traction.

NCT ID: NCT04451109 Enrolling by invitation - Clinical trials for Gestational Diabetes

Dilapan-S®: A Multicenter US E-registry

Start date: December 1, 2020
Phase:
Study type: Observational

Objective of this registry is to collect a representative set of real world data on the use of Dilapan-S® for pre-induction cervical ripening in daily clinical practice. Upon completion of the registry, relevant collected data will be analyzed and published.

NCT ID: NCT04569643 Enrolling by invitation - Clinical trials for Cognitive Dysfunction

Periodic Limb Movement Syndrome in Patients With Cerebral Small Vessel Disease.

Start date: December 1, 2020
Phase:
Study type: Observational

Patients from 60 to 75 years old diagnosed with cerebral small vessel disease with no history of symptomatic stroke, brain tumor, traumatic brain injury, seizures and neurodegenerative or mental disorder will undergo overnight leg actigraphy and cardiorespiratory monitoring. Those of them with apnea/hypopnea index under 5 will be enrolled. Brain MRI and cognitive assessment will be performed at baseline and in 1-year follow-up, sleep quality will be assessed at baseline with self-reported questionnaires. Progression of cerebral small vessel disease markers and cognitive dysfunction will be compared between patients with high periodic limb movement index (the number of periodic limb movement ≥ 15 per hour of sleep) and controls (periodic limb movement index < 15/h).

NCT ID: NCT04640727 Enrolling by invitation - Humeral Fractures Clinical Trials

ORIF Versus CRIF of Completely Displaced and Rotated Lateral Condylar Fractures of the Humerus in Children

Start date: December 1, 2020
Phase:
Study type: Observational

Open reduction and internal fixation has been widely used in treating completely displaced and rotated lateral condylar fracture in children and it usually produces good results. Only a few studies reported Closed reduction and internal fixation is an effective treatment for completely displaced and rotated lateral condyle fractures of the humerus, but evidence on its effectiveness and safety is scarce. The aim of the trial was to compare functional and outcome use in patients treated completely displaced and rotated lateral condylar fracture with ORIF versus CRIF.