NCT00689494

UnknownPhase 1/2

Cervical Device Contraception-2 (Nanopaz)

Bnai Zion Medical Center Source

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Other study identifiers

Sponsor study identifier

BnaiZionMC-08-BP-003-CTIL

Study Type

interventional

Estimated enrollment

10

Locations

0 countries

Sites

N/A

Timeline

Study Start

June 2008

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

December 2008

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Study Completion

May 2010

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Brief Summary

Measure blood progesterone by using cervical device contraception.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: unknown
Estimated enrollment: 10 participants
Study completion date: May 2010
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.
Listed locations: 0 countries · 0 sites

Trial Relationships

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Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

First Submitted
May 19, 2008
Actual (reported)
Study Start
June 2008
Date type not reported
This date has not been verified as actual or estimated.
First Posted
June 3, 2008
Actual (reported)
Primary Completion
December 2008
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.
Study Completion
May 2010
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.

Last Updated: June 3, 2008
Status Verified: June 2008
Last Update Submitted: June 2, 2008

Conditions

Healthy

Keywords

Nanopaz deviceBlood progesterone measure in using the deviceDelivery progesteroneProgesterone levonorgestrel

Outcome Measures

Primary Outcomes (1)

blood progesterone measure in blood
one to two months

Interventions

Nanopaz contraception deviceOther

levonorgestrel and levonorgestrel device for cervical contraception-nantechnolgy method

Also known as: levonorgestrel device for cervical contraception-nantechnolgy method

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age1 Month - 2 Months

Sexfemale

Healthy VolunteersYes

Age GroupsChild (0-17)

You may qualify if:

healthy women are candidate for hysterectomy

You may not qualify if:

Sponsors & Collaborators

Bnai Zion Medical Center
Governmentlead

Study Design

Study Type: interventional
Phase: phase 1 2
Allocation: NON RANDOMIZED
Masking: NONE
Purpose: PREVENTION
Intervention Model: SINGLE GROUP
Sponsor Type: OTHER GOV

Study Record Dates

First Submitted

May 19, 2008

First Posted

June 3, 2008

Study Start

June 2008

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

December 2008

Estimated (date passed)

Phase 1/2

Unknown

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Contact the study team to confirm eligibility.

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Study Completion

May 2010

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Last Updated

June 3, 2008

Record last verified: 2008-06

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT00689494
Data provider: ClinicalTrials.gov
Source updated: 2008-06-03
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:23:40 UTC

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

Study Start

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Design

Study Record Dates

Source record