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NCT ID: NCT02272413 Completed - Clinical trials for Carcinoma, Non-Small-Cell Lung

Phase III Trial BI 695502 Plus Chemotherapy vs. Avastin® Plus Chemotherapy in Patients With Lung Cancer

Start date: July 8, 2015
Phase: Phase 3
Study type: Interventional

The objective of this phase III trial is to establish statistical equivalence in terms of efficacy (best overall response rate [ORR], proportion of patients with complete response [CR] plus partial response [PR]) until 18 weeks of first-line treatment with BI 695502 plus chemotherapy versus Avastin® plus chemotherapy followed by maintenance monotherapy with either BI 695502 or Avastin®.

NCT ID: NCT02271646 Completed - Liver Cancer Clinical Trials

Ultrasound Guided Thoracic Paravertebral Block for Hepatic Tumors Ablation

Start date: August 2014
Phase: N/A
Study type: Interventional

Patients undergo percutaneous radiofrequency ablation of hepatic tumors at Siriraj hospital normally receive only intravenous sedative drugs which sometimes can not provide effective pain control. TPVB is suitable for unilateral operations. And it is increasing popular nowadays because of using ultrasound guided which make it is more reliable and has less side effects especially the severe one such as pneumothorax. To cover all nerve supply liver, we decided to use right TPVB at T5-6, T7-8, and T9-10. The aim of this study is to prove that TPVB can provide an effective pain control for patients undergo liver RFA both at rest and movement (cough). We are going to measure the pain score at recovery room and the effective pain control means patients has mild pain (pain score less </= 3 and do not ask for analgesic drugs).

NCT ID: NCT02271620 Completed - Clinical trials for Other Allergic Rhinitis

The Prevalence and Clinical Characteristics of Children With Local Allergic Rhinitis

Start date: January 2014
Phase: N/A
Study type: Interventional

- To determine prevalence of local allergic rhinitis (LAR) - To evaluate clinical characteristic and severity of local allergic rhinitis - To measure changing of tryptase and Specific IgE for Dermatophagoides pteronyssinus (Dp) after nasal allergen provocation test (NAPT)

NCT ID: NCT02270294 Completed - Ischemic Stroke Clinical Trials

Acute Effects of Thai Traditional Massage on Cerebrovascular Reactivity in Ischemic Stroke Patients

Start date: October 1, 2014
Phase: N/A
Study type: Interventional

The investigators hypothesize that Acute Thai traditional massage will yield beneficial effects on cerebrovascular reactivity in ischemic stroke patients.

NCT ID: NCT02267824 Completed - Malocclusion Clinical Trials

The Effects of Extraoral Photobiomodulation on the Rate of Orthodontic Alignment

Start date: December 2010
Phase: N/A
Study type: Interventional

The aim of this study is to determine if extraoral OrthoPulse®, which emits extraoral LED (Light Emitting Diode) photobiomodulation (PBM), reduces the time it takes to complete orthodontic alignment.

NCT ID: NCT02266264 Completed - Hyperglycemia Clinical Trials

Hyperglycemia and Effects of Daily 100 mg Versus 200 mg of Hydrocortisone Therapy in Patients With Septic Shock

Start date: October 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare hyperglycemia and other effects, include 28-day mortality and time to reversal of shock between 100 milligrams and 200 milligrams of hydrocortisone as initial dosage in patients with septic shock.

NCT ID: NCT02263443 Completed - Clinical trials for Other Surgical Procedures

Appropriated Bowel Preparation Before Exploratory Laparotomy in Gynecologic Surgery

Start date: October 2014
Phase: N/A
Study type: Interventional

Our study perform In Department of Gynecology, Faculty of Medicine, Chiang Mai University. In our study we divide patients into 3 groups ,First group patients doing Soap suds enema (S.S.E.), second group patients doing sodium chloride enema and the last group patient Non per os (NPO) before surgery. Our hypothesis is no different about surgical view in 3 groups and lower side effects in patients in no bowel preparation group. Research objectives 1. Comparing the surgeon satisfaction ,surgical view and bowel handling in operation of soap suds enema group, sodium chloride enema group and the NPO group in patients under going exploratory laparotomy in gynecologic surgery. 2. Comparing the side effects of soap suds enema group, sodium chloride enema group and the NPO group. Inclusion Criteria 1. Women under going laparotomy in gynecologic surgery 2. Surgeon consider not too difficult surgery. 3. Can understanding Thai language. 4. Can communicate with researcher. 5. Consenting participants. Exclusion Criteria 1. Pregnancy or suspected pregnancy. 2. Laparoscopic surgery 3. Do not consent to participate in research 4. Gastrointestinal infection 5. Underlying disease such as Intestinal disease, patient who cannot under going bowel preparation ,heart disease ,seizure. 6. Surgeon consider difficult surgery such as fixed mass or uterus with others organs from per vaginal examination or very huge mass or history of difficult surgery or history of severe adhesion in abdominal cavity.

NCT ID: NCT02262975 Completed - Alzheimer's Disease Clinical Trials

A Multi-national Study to Identify Treatment Discontinuation Rate in de Novo Alzheimer's Disease Patients Who Have Been Newly Prescribed With Donepezil (Aricept) in Asia (ADOS)

ADOS
Start date: July 2014
Phase: N/A
Study type: Observational

This study is an observational study conducted prospectively under routine clinical setting for 1 year with about 700 patients diagnosed as Alzheimer's disease who will be treated by donepezil (Aricept) as monotherapy. The subjects will be recruited in the selected institutions of about 8 countries in Asia.

NCT ID: NCT02262481 Completed - Preterm Labor Clinical Trials

Oral Progestogen Supplementation in the Prevention of Recurrent Uterine Contraction in Preterm Labor

Start date: August 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of oral progesterone supplementation in preterm labor on the prevention of recurrent uterine contraction and prolonging pregnancy period, and its side effect.

NCT ID: NCT02253381 Completed - Hypotension Clinical Trials

Effect of Position During Spinal Anesthesia on Hemodynamic Change in Cesarean Section

Start date: October 2014
Phase: N/A
Study type: Interventional

Hypotension is the most common complications after spinal anesthesia especially in pregnant patients who undergoing cesarean section. Position during spinal anesthesia may be altering the hemodynamic. For right lateral decubitus, the enlarged uterus compresses inferior vena cava that may decrease venous return and cardiac output. This leads to hypotension.The hypothesis is the right lateral position during spinal anesthesia in pregnant women will be had hemodynamic changing more than the left lateral position. This objective is to compare hemodynamic change between left and right lateral position during spinal anesthesia in pregnant women undergoing cesarean section.