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Completed

NCT Number: NCT03769584

Follow-up of Treatment Outcome, Quality of Life, Sexual Life and Partnership After Surgery of Endometriosis

Follow-up of treatment outcome, quality of life, sexual life and partnership after surgery of endometriosis by means of a questionnaire 1 year after surgical Intervention.

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Key information

Conditions

Endometriosis Behavior Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Genital Diseases Genital Diseases, Female Sexual Behavior Sexuality Urogenital Diseases

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Frauenklinik University Hospital Basel

Basel, 4031, Switzerland

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • surgery of endometriosis at Frauenklinik of University Hospital Basel (from 01.01.2017 until 31.12.2017)
  • sufficient German language skills in order to be able to complete questionnaires

Exclusion criteria

  • incapable of consenting

Treatment and study plan

Follow-up Questionnaire

Other

Online- Questionnaire investigating Follow-up of Treatment Outcome, Quality of Life, Sexual Life and Partnership After Surgery of Endometriosis

Follow- up interview

Other

Semi- structured Interview investigating Follow-up of Treatment Outcome, Quality of Life, Sexual Life and Partnership After Surgery of Endometriosis

Primary outcomes

  1. Endometriosis- associated symptoms assessed by questionnaire

    Time frame: 1 year after surgery of endometriosis

    questionnaire asking for pain (with menstruation, with sexual intercourse, with defecation, with urination) on a Visual Analogue Scale (VAS), ranging from 0 = no pain to 10 = intolerable pain

  2. Treatment outcome of surgery of endometriosis assessed by VAS questionnaire

    Time frame: 1 year after surgery of endometriosis

    questionnaire asking for satisfaction with treatment outcome on a Visual Analogue Scale (VAS), ranging from 0 = absolutely dissatisfied to 10 = absolutely satisfied

  3. Change in Quality of life assessed by questionnaire

    Time frame: before surgery of endometriosis and 1 year after surgery of endometriosis

    questionnaire asking for Quality of life on a Visual Analogue Scale (VAS), ranging from 0 = very bad to 10 = very good

  4. Change in sexual life assessed by questionnaire

    Time frame: before surgery of endometriosis and 1 year after surgery of endometriosis

    questionnaire asking for Sexual life on a Visual Analogue Scale (VAS), ranging from 0 = absolutely dissatisfied to 10 = absolutely satisfied

  5. Change in conduct of life assessed by questionnaire

    Time frame: before surgery of endometriosis and 1 year after surgery of endometriosis

    questionnaire asking for change in conduct of life (partnership, family, professional life, leisure activity, sportive activities) on a 6- item scale (ranging from "negative" to "positive")

  6. Change in wish for child assessed by questionnaire

    Time frame: before surgery of endometriosis and 1 year after surgery of endometriosis

    questionnaire asking for change in wish for child on a 3- item scale (ranging from "yes" , "no answer" to "no")

Secondary outcomes

  1. Follow-up of Treatment outcome of surgery of endometriosis assessed by interview

    Time frame: 1 year after surgery of endometriosis

    semi- structured interview to assess comments of study participants that are not depicted in the questionnaires

Sponsors and collaborators

Lead sponsor

University Hospital, Basel, Switzerland

Other

Registry information

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Dec 7, 2018
Registry last updated
Jan 30, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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