Effects of Glucagon-like-Peptide-1 Analogues on Sexuality

NCT ID: NCT05598008

Last Updated: 2025-12-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

85 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-11-25

Study Completion Date

2025-10-24

Brief Summary

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This study is to investigate the effects of GLP-1 analogues (combined with lifestyle interventions in comparison to lifestyle interventions only) on sexual desire, mood, quality of life, the reproductive axis, retinal vessel diameters, physical fitness (and semen, for men only) in overweight or obese men and women.

Detailed Description

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Glucagon-like peptide-1 (GLP-1) analogues are widely used for the treatment of type 2 diabetes mellitus due to its well-known insulinotropic effects as well as for the treatment of obesity due to its satiation-promoting and appetite- suppressant effects. The GLP-1 analogues are approved in patients with obesity (BMI ≥ 30 kg/m2) or who are overweight (BMI ≥ 27 kg/m2) with additional comorbidities, such as prediabetes, diabetes mellitus type 2, arterial hypertension or dyslipidemia. Beside its influence on the reward for palatable food, several studies have shown that GLP-1 analogues modulate the rewarding effects of addictive drugs such as alcohol, nicotine and cocaine. As a further natural reward, sexual desire could be affected by GLP-1 analogues likewise.

This study investigates the influence of GLP-1 analogues on sexuality in a population of overweight and obese participants. A treatment with a GLP-1 analogue combined with lifestyle modifications for weight reduction will be compared to weight reduction with conventional lifestyle modifications only. In the context of the increasing use of GLP-1 analogues, particularly in young people with reproductive desire, laboratory analyzes of the reproductive axis (hormones and sperm cells) will be part of this study to document a possible influence. Mood changes, physical activity and fitness and effects on microvascular endothelial functioning by measuring diameters of retinal vessels will be further investigated.

Conditions

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Sexual Desire

Keywords

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Glucagon-like-Peptide-1 (GLP-1) Glucagon-like peptide-1 (GLP-1) analogues obesity sexuality Liraglutide (Saxenda®) obese men reproductive axis microvascular endothelial function retinal vessels physical activity physical fitness mood sperm cells

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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GLP-1 Group

GLP-1 Group: receiving GLP-1 analogues for weight management in addition to conventional weight management (= lifestyle intervention plus GLP-1 analogues).

Conventional weight management is conducted according to clinical guidelines (in both groups) and includes nutritional and exercise counselling, counselling by motivational coaches and/ or psychological support.

Participants in the GLP-1 group will inject the medication themselves.

No interventions assigned to this group

Lifestyle group

Lifestyle group: using conventional weight management (= lifestyle intervention only).

Conventional weight management is conducted according to clinical guidelines (in both groups) and includes nutritional and exercise counselling, counselling by motivational coaches and/ or psychological support.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* BMI ≥ 27 kg/m2
* Willingness to lose weight by lifestyle changes only or by lifestyle changes plus GLP-1 analogue treatment as agreed in a routine clinical appointment
* Active sex life (sex with partner or masturbation ≥2x/month)
* Eugonadism:

* Men: morning total testosterone ≥12mmol/l or free testosterone ≥ 0.198 nmol/l if\< 50 years old and ≥ 0.163 if \> 50 years old
* Women: no primary or secondary amenorrhea (inclusive menopause) \*Secondary amenorrhea is defined as "absence of menses for more than three months in women who previously had regular menstrual cycles or six months in women who had irregular menses".

Exclusion Criteria

* Diabetes mellitus, HbA1c ≥ 6,5 %
* Previous use of GLP-1 analogues during last 2 months.
* Exogenous testosterone substitution
* Current illicit drug abuse
* Pregnancy
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Swiss National Science Foundation

OTHER

Sponsor Role collaborator

University Hospital, Basel, Switzerland

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Bettina Winzeler, Dr. med.

Role: PRINCIPAL_INVESTIGATOR

Endocrinology, Diabetes and Metabolism, University Hospital Basel

Locations

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University Hospital Basel, Endocrinology, Diabetes and Metabolism

Basel, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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2022-01367; kt22Winzeler

Identifier Type: -

Identifier Source: org_study_id