Evaluation of patient satisfaction with skin adhesive (Liquiband) for wounds after gynecological laparoscopic surgery, randomized controlled trial with hydrocolloid preparation (Clear Hessive)

Evaluation of patient satisfaction with skin adhesive (Liquiband) for wounds after gynecological laparoscopic surgery, randomized controlled trial with hydrocolloid preparation (Clear Hessive) - Evaluation of patient satisfaction with skin adhesive for wounds after gynecological laparoscopic surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000037690

Enrollment

Registered

2019-09-01

Start date

2019-09-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

leiomyomas or benign ovarian tumors

Interventions

Skin adhesive Hydrocolloid formulation

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Patients scheduled to undergo laparoscopic surgery for leiomyomas or ovarian benign tumors

Exclusion criteria

Exclusion criteria: Pregnant or diabetic

Design outcomes

Primary

Measure	Time frame
patient satisfaction	—

Countries

Japan

Contacts

Public ContactRie Ozaki

Juntendo University Faculty of Medicine Obstetrics and Gynecology

rieozaki@juntendo.ac.jp0338133111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026