Effectiveness of the Use of the PICSI Dish (Hyaluronan Microdot) in

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment

See also
Status	Clinical Trial	Phase
Not yet recruiting	`NCT03978013` - Pomegranate Juice Effect on Oxidative Stress in Infertile Women During IVF Treatment	N/A
Recruiting	`NCT05885516` - Double vs Single Intrauterine Insemination in Male Factor Infertility	N/A
Completed	`NCT01661010` - The Clinical Study of Sex Chromosome Variants
Recruiting	`NCT02992665` - Can Calcium Ionophore Application Enhance the ICSI Outcomes in Severe Male Factor Infertility?	Phase 2/Phase 3

See also

Status

Clinical Trial

Phase

Not yet recruiting

NCT03978013 - Pomegranate Juice Effect on Oxidative Stress in Infertile Women During IVF Treatment

N/A

Recruiting

NCT05885516 - Double vs Single Intrauterine Insemination in Male Factor Infertility

N/A

Completed

NCT01661010 - The Clinical Study of Sex Chromosome Variants

Recruiting

NCT02992665 - Can Calcium Ionophore Application Enhance the ICSI Outcomes in Severe Male Factor Infertility?

Phase 2/Phase 3

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT00741494
Study type	Interventional
Source	Biocoat
Contact
Status	Completed
Phase	N/A
Start date	August 2008

Effectiveness of the Use of the PICSI Dish (Hyaluronan Microdot) in the Selection of Sperm for Intracytoplasmic Sperm Injection (ICSI)

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms