Clinical trials for evaluation of efficacy of a chitosan tampon (Hemoblock-Tampon) in preventing hemorrhage after the loop electrosurgical excision procedure

Data collection for hemostasis and function of Chito HEMOBLOCK (Tampon) after loop electrosurgical excision procedure

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CRIS

Registry ID

KCT0003696

Enrollment

Registered

2019-04-01

Start date

2017-12-05

Completion date

Unknown

Last updated

2019-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device, Procedure/Surgery : Chitosan tampon was applied to the uterine cervix immediately after LEEP surgery in the treatment group, and general tampon made of cotton was applied to the uterin

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: The inclusion criteria were - Age 20–65 years - Biopsy-confirmed CIN grade =2, - Appropirate medical condition for LEEP - Provision of informed written consent for participation.

Exclusion criteria

Exclusion criteria: The exclusion criteria were - Inappropiate medical condition for loop - Pregnant status - Patients who denied participation of clinical trial. - Hpersensitivity to crustacean foods were excluded.

Design outcomes

Primary

Measure	Time frame
Postoperative bleeding using a pictorial blood loss assessment chart	—

Secondary

Measure	Time frame
quality of life	—

Countries

Korea, Republic of

Contacts

Public ContactGun Oh Chong

Kyungpook National University Medical Center

oh-gun@hanmail.net+82-53-200-2684

Outcome results