UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022490
Receipt number R000025916
Scientific Title Non-randomized, single arm study of the efficacy of a temporary insertion of intrauterine silicone plate for preventing intrauterine adhesion after hysteroscopic surgery.
Date of disclosure of the study information 2016/05/30
Last modified on 2023/06/08 09:47:01

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Basic information

Public title

Non-randomized, single arm study of the efficacy of a temporary insertion of intrauterine silicone plate for preventing intrauterine adhesion after hysteroscopic surgery.

Acronym

A study of the efficacy of a temporary insertion of intrauterine silicone plate for preventing intrauterine adhesion after hysteroscopic surgery.

Scientific Title

Non-randomized, single arm study of the efficacy of a temporary insertion of intrauterine silicone plate for preventing intrauterine adhesion after hysteroscopic surgery.

Scientific Title:Acronym

A study of the efficacy of a temporary insertion of intrauterine silicone plate for preventing intrauterine adhesion after hysteroscopic surgery.

Region

Japan


Condition

Condition

Intrauterine Adhesion (Asherman syndrome), Uterine septum.

Classification by specialty

Obstetrics and Gynecology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To Investigate the efficacy of a temporary insertion of intrauterine silicone plate for preventing intrauterine adhesion after surgery.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Intrauterine adhesion rate after one year following hysteroscopic surgery for preventing intrauterine adhesion.

Key secondary outcomes

Intrauterine adhesion rate after two months following hysteroscopic surgery for preventing intrauterine adhesion.
Pregnancy rate after one year following hysterscopic surgery for preventing intrauterine adhesion.


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Insertion of intrauterine silicone plate.

Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit


Not applicable

Age-upper limit

49 years-old >=

Gender

Female

Key inclusion criteria

1.Intrauterine adhesion(Asherman syndrome) ,Uterine septum
2. Infertility or Recurrent pregnancy loss
3.Patients who plan to undergo hysteroscopic adhesiolysis or hysteroscopic uterine septum resection

Key exclusion criteria

1.Women who don't desire to conceive
2.Patients with severe immunocompromised state

Target sample size

15


Research contact person

Name of lead principal investigator

1st name Yoichi
Middle name
Last name Aoki

Organization

University of the Ryukyus

Division name

Graduate School of Medical Science University of the Ryukyus

Zip code

9030215

Address

207 Uehara, Nishihara, Okinawa

TEL

098-895-1177

Email

yoichi@med.u-ryukyu.ac.jp


Public contact

Name of contact person

1st name Keiko
Middle name
Last name Mekaru

Organization

University of the Ryukyus Hospital

Division name

Obstetrics and gynecology

Zip code

9030215

Address

207 Uehara, Nishihara, Okinawa

TEL

098-895-1177

Homepage URL


Email

f041252@eve.u-ryukyu.ac.jp


Sponsor or person

Institute

University of the Ryukyus

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Review Board of University of the Ryukyus for Clinical Research

Address

207 Uehara, Nishihara, Okinawa

Tel

098-895-8016

Email

knknkyu@to.jim.u-ryukyu.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2016 Year 05 Month 30 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Enrolling by invitation

Date of protocol fixation

2016 Year 04 Month 04 Day

Date of IRB

2016 Year 04 Month 04 Day

Anticipated trial start date

2016 Year 05 Month 30 Day

Last follow-up date

2027 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2016 Year 05 Month 27 Day

Last modified on

2023 Year 06 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000025916


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name