Endometrial Polypectomy Performed With Bipolar Electrode Versapoint vs Microscissors or Graspers

Comparative Study of Endometrial Polypectomy Performed With Bipolar Electrode Versapoint vs Microscissors or Graspers

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02590666

Enrollment

Registered

2015-10-29

Start date

2016-06-30

Completion date

2017-09-30

Last updated

2016-03-09

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

Conditions

Endometrial Polyps

Brief summary

Hysteroscopy today is considered the gold standard for the diagnosis and treatment of endometrial polyps. Several hysteroscopic systems to resect endometrial polyps are currently available. Among Others bipolar systems and microscissors or graspers, both of theme make part of routine clinical practice and are universally accepted. The aim of the study is to compare the efficacy of bipolar resection energy polypectomy versus microscissors or graspers These procedures assume a lower cost and are associated with a lower surgical risk due to their realization without anesthesia . Hypothesis: Resection of polyps outpatient laser diode has a similar or superior to that of the bipolar electrode tolerability. The diode laser is a viable , quick , simple technique with a high percentage of resection and high degree of satisfaction of patients

Interventions

PROCEDUREBipolar Polypectomy

Polyps resection with bipolar electrode

PROCEDUREMechanical Polypectomy

Polyps resection with microscissors or graspers

DEVICEBipolar electrode

Bipolar electrode used to performs polypectomy

DEVICEMicroscissors or graspers

Mechanical instruments used to performs polypectomy

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 60 Years

Healthy volunteers

Yes

Inclusion criteria

* The patient must be informed about the study, and sign the informed consent

Exclusion criteria

* Positive Pap smear test * Pregnancy * Uterine malignancy * Abnormal uterine bleeding

Design outcomes

Primary

Measure	Time frame
To assess the tolerability of polypectomy using a validated visual analogue pain scale	we measure pain after resection of endometrial polyps, with 5 minutes for the patient thinks

Other

Measure	Time frame
Assess the recurrence of polyps after 3 months of resection (another hysteroscopy).	3 months after resection of the polyp, repeat hysteroscopy to assess recurrence

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026