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NCT ID: NCT00785785 Completed - Clinical trials for Gastrointestinal Stromal Tumor (GIST)

A Study of Nilotinib Versus Imatinib in GIST Patients

ENESTg1
Start date: March 2009
Phase: Phase 3
Study type: Interventional

This study will evaluate efficacy and safety of nilotinib versus imatinib in adult patients with unresectable or metastatic gastrointestinal stromal tumors (GIST).

NCT ID: NCT00785720 Completed - Hygiene Clinical Trials

Dermacyd PH_DETINBACK (Lactic Acid) Sweet Flower - Photo Avaluation

Start date: August 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate the absence of photoirritation and photosensitization potential of the product Dermacyd PHDETINBACK Sweet Flower.

NCT ID: NCT00785681 Completed - Hygiene Clinical Trials

Dermacyd PH_DETINBACK (Lactic Acid) Sweet Flower - Compatibility

Start date: July 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate the absence of irritation potential (primary dermical irritability and cumulated dermical irritability) and allergy (sensibilization) of the product Dermacyd PHDETINBACK Sweet Flower.

NCT ID: NCT00785655 Completed - Hygiene Clinical Trials

Dermacyd PH_DETINLYN (Lactic Acid) Sweet Flower - Compatibility

Start date: July 2008
Phase: Phase 3
Study type: Interventional

To demonstrate the absence of irritation potential (primary dermical irritability and cumulated dermical irritability) and allergy (sensibilization) of the product Dermacyd PHDETINLYN Sweet Flower.

NCT ID: NCT00785642 Completed - Hygiene Clinical Trials

Dermacyd PH_DETINLYN Tangerine Mix (Lactic Acid) - Safety.

Start date: August 2008
Phase: Phase 3
Study type: Interventional

To prove the safety of the gynaecological formulation in normal conditions of use.

NCT ID: NCT00785590 Completed - Hygiene Clinical Trials

Dermacyd PH_DETINLYN (Lactic Acid) Sweet Flower - Photo Evaluation.

Start date: August 2008
Phase: Phase 3
Study type: Interventional

To demonstrate the absence of photoirritation and photosensitization potential of the product Dermacyd PHDETINLYN Sweet Flower.

NCT ID: NCT00785148 Completed - Hygiene Clinical Trials

Dermacyd PH_DETINLYN Sweet Flower (Lactic Acid) - Safety

Start date: August 2008
Phase: Phase 3
Study type: Interventional

To prove the safety of the gynaecological formulation in normal conditions of use.

NCT ID: NCT00784160 Completed - Hygiene Clinical Trials

Dermacyd PH_DETINBACK Tangerine Mix (Lactic Acid)- Compatibility

Start date: July 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate the absence of irritation potential (primary dermic irritability and cumulated dermic irritability) and allergy (sensibilization) of the product Dermacyd PHDETINBACK Tangerine Mix (Lactic Acid).

NCT ID: NCT00784134 Completed - Clinical trials for Intraventricular Hemorrhage

Clot Lysis: Evaluating Accelerated Resolution of Intraventricular Hemorrhage Phase III

CLEAR III
Start date: July 2009
Phase: Phase 3
Study type: Interventional

The overall objective of this Phase III clinical trial is to obtain information from a population of 500 ICH subjects with intraventricular hemorrhage (IVH), representative of current clinical practice and national demographics of ICH regarding the benefit (or lack thereof) of IVH clot removal on subject function as measured by modified Rankin Scale (mRS). This application requests funding for five years to initiate a Phase III randomized clinical trial (RCT) testing the benefit of clot removal for intraventricular hemorrhage. The investigators propose to compare extraventricular drainage (EVD) use plus recombinant tissue plasminogen activator (rt-PA; Alteplase; Genentech, Inc., San Francisco, CA) with EVD+ placebo in the management and treatment of subjects with small intracerebral hemorrhage (ICH) and large intraventricular hemorrhage (IVH defined as ICH < 30 cc and obstruction of the 3rd or 4th ventricles by intraventricular blood clot).

NCT ID: NCT00784121 Completed - Hygiene Clinical Trials

Dermacyd Breeze (Lactic Acid) Pocket BR - Compatibility

Start date: October 2008
Phase: Phase 3
Study type: Interventional

To demonstrate the absence of irritation potential (primary dermic irritability and cumulated dermic irritability) and allergy (sensibilization) of the product Dermacyd Breeze (Lactic Acid) Pocket BR.