Comparison of the adhesion-preventative effect of HaemoCer PLUS and isotonic saline solution after endometriosis treatment using transvaginal sonography.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00038010

Enrollment

Registered

2026-01-28

Start date

2025-10-14

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

N80.3 N80.1 N80.2 N80.4

Interventions

Group 1: The operation for complete endometriosis removal is performed according to the clinic's general treatment standards. Intervention group: After removal of the endometriosis, HaemoCer PLUS is a

Eligibility

Sex/Gender

Female

Age

18 Years to 50 Years

Inclusion criteria

Inclusion criteria: • Suspicion of moderate to severe endometriosis (at least stage II endometriosis according to rASRM) • Existing uterus

Exclusion criteria

Exclusion criteria: • Pregnant patients • Intestinal endometriosis • Known intolerance to starch or starch containing products

Design outcomes

Primary

Measure	Time frame
Three months after endometriosis surgery, an ultrasound scan is performed to assess adhesions in various areas of the lower abdomen using the sliding sign. Adhesions are classified into four stages: no adhesions (0 points), minor adhesions (1 point), numerous adhesions (2 points) and severe adhesions (3 points). The individual scores are summed up, and the totals for both study arms are compared pre- and postoperatively.	—

Measure

Time frame

Three months after endometriosis surgery, an ultrasound scan is performed to assess adhesions in various areas of the lower abdomen using the sliding sign. Adhesions are classified into four stages: no adhesions (0 points), minor adhesions (1 point), numerous adhesions (2 points) and severe adhesions (3 points). The individual scores are summed up, and the totals for both study arms are compared pre- and postoperatively.

—

Secondary

Measure	Time frame
The following secondary endpoints will be assessed during the follow-up examination three months after surgery: • Postoperative pain • Postoperative complications • Postoperative ovarian volume • Postoperative uterine volume • Endometriosis-specific symptoms • Postoperative inflammation parameters	—

Countries

Germany

Contacts

Public ContactRazvan Petru Derihaci

Klinik und Poliklinik für Frauenheilkunde und Geburtshilfe Universitätsklinikum Carl Gustav Carus

RazvanPetru.Derihaci@uniklinikum-dresden.de+49 351 458 3420

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 7, 2026