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The Effect of Ligasure® to Destroy Cornual Portion of Fallopian Tube

Samsung Medical Center logo

Samsung Medical Center

Status and phase

Completed
Phase 3

Conditions

Completed
Recruiting

Treatments

Device: The Effect of Ligasure® to Destroy Cornual Portion of Fallopian Tube

Study type

Interventional

Funder types

Other

Identifiers

NCT01894971
2013-06-25

Details and patient eligibility

About

Single-center prospective randomized trial to evaluate the effect of thermal damage of Ligasure® to destroy cornual portion of fallopian tube tisse.

Right of Left side of fallpian tube is randomized and coagulated one more time than other side before cut off. The pathologist evaluate the amount of fallopian tube tissue left at both cornual portion of cut off specimen.

Full description

When investigators perform salpingectomy, both side of cornual portion of the uterus are coagulated by Ligasure®. The randomized, the same word selected side of the fallopian tube is coagulated one more time at the cornual portion than unselected other side of fallopian tube. Hypothesis is that the side selected and coagulated twice would have less fallopian tube tisse left at fianl pathology than the side only once coagulated by Ligasure®.

Enrollment

40 patients

Sex

Female

Ages

35 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • female 35-50
  • premenopausal
  • plan to perform hysterectomy

Exclusion criteria

  • disease in fallopian tube before surgery
  • has history of pelvic inflammatory disease

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

Double Blind

40 participants in 1 patient group

twice coagulated side of fallopian tube
Experimental group
Description:
twice coagulated side of fallopian tube once coagulated sied of fallopian tube
Treatment:
Device: The Effect of Ligasure® to Destroy Cornual Portion of Fallopian Tube

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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