Other Clinical Trial - Observational vs. Ablative Treatment for Low-grade

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

LSIL, Low-Grade Squamous Intraepithelial Lesions
Squamous Intraepithelial Lesions of the Cervix

See also
	Status	Clinical Trial	Phase
	Recruiting	`NCT05051852` - HPV Viral Load in Predicting the Prognosis of LSIL
	Recruiting	`NCT05283239` - Research About Impact of HPV Integration on the Prognosis of Women With Persistent HR-HPV Infection

See also

Status

Clinical Trial

Phase

Recruiting

NCT05051852 - HPV Viral Load in Predicting the Prognosis of LSIL

Recruiting

NCT05283239 - Research About Impact of HPV Integration on the Prognosis of Women With Persistent HR-HPV Infection

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	NCT02331550
Study type	Interventional
Source	Saint Thomas Hospital, Panama
Contact
Status	Completed
Phase	N/A
Start date	January 2014
Completion date	December 2014

Observational vs. Ablative Treatment for Low-grade Squamous Intraepithelial Lesions.

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms