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NCT05730205 · ClinicalTrials.gov registry record · Phase 4

Effects of the Contraceptive Implant in Women With Sickle Cell Disease

A Phase 4 study of Sickle Cell Disease, sponsored by University of Pennsylvania.

Recruiting
Registry status
Phase 4
Development phase
22
Enrollment target
1
Study location

NCT05730205 is a Phase 4 study of Sickle Cell Disease that is actively recruiting participants, run by University of Pennsylvania. The registered enrollment target is 22 participants, below the 293-participant average among 213 other Sickle Cell Disease trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05730205, a Phase 4 study of Sickle Cell Disease, is actively recruiting participants, sponsored by University of Pennsylvania.

RECRUITING
Registry status
Phase 4
Development phase
22 participants
Enrollment target
1
Study location

Study Summary

The objective of this study is to measure the acceptability and impact of the progestin implant on frequency of vaso-occlusive crises, quality of life, and hematologic parameters in women with SCD.

Conditions Studied

Interventions

  • DRUG Nexplanon 68 MG Drug Implant

Study Locations (1)

Pennsylvania

  • Penn Medicine University City - Philadelphia

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2023-06-08
Est. Completion 2026-06-15
Phase Phase 4

Sponsor

University of Pennsylvania

1,423 total trials

What the Registry Record Tells You About NCT05730205

The ClinicalTrials.gov registry entry for NCT05730205 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 22 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 293-participant average among 213 other Sickle Cell Disease trials with a reported enrollment target (92% lower). The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Sickle Cell Disease appearing as the primary indexed condition, and to 1 intervention - of which Nexplanon 68 MG Drug Implant is the first listed.

NCT05730205 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT05730205 about?

NCT05730205 is a clinical study titled "Effects of the Contraceptive Implant in Women With Sickle Cell Disease". The objective of this study is to measure the acceptability and impact of the progestin implant on frequency of vaso-occlusive crises, quality of life, and hematologic parameters in women with SCD.

What is the current status of trial NCT05730205?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 22 participants. The study started on 2023-06-08. Estimated completion is 2026-06-15.

What conditions does trial NCT05730205 study?

This clinical trial studies the following conditions: Sickle Cell Disease.

What interventions are being tested in trial NCT05730205?

The interventions under investigation include: Nexplanon 68 MG Drug Implant (DRUG).

Who is sponsoring clinical trial NCT05730205?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05730205 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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