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Integral microwave magnetic therapeutic apparatus of male sexual dysfunction ED patients curative effect and safety evaluation

Integral microwave magnetic therapeutic apparatus of male sexual dysfunction ED patients curative effect and safety evaluation: A randomized, double-blind, controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019320
Enrollment
Unknown
Registered
2018-11-06
Start date
2018-11-01
Completion date
Unknown
Last updated
2018-11-19

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

Conditions

erectile dysfunction

Interventions

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
22 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) Patients with erectile dysfunction more than 6 months; (2) Aged 22 to 50 years; (3) Stable heterosexual relationship for more than 6 months; (4) Signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with history of alcoholism or drug abuse; (2) Patients with abnormal anatomy of the penis wich will cause severe erectile dysfunction; (3) Patients with primary low sexual desire; (4) Patients with erectile dysfunction caused by spinal injury; (5) Patients with history of prostatectomy; (6) Within 6 months before the trial, patients had a history of unstable angina, heart failure, myocardial infarction, stroke, life-threatening arrhythmia or with pacemaker; (7) Patients with active gastrointestinal ulcer, bleeding disorders and abnormal liver and kidney function; (8) Patients with hypotension at rest (systolic blood pressure at rest 170 mmHg or diastolic blood pressure > 110 mmHg); (9) Patients taking nitrate or nitric oxide precursor drugs; (10) Fasting blood glucose in diabetics is 1.2 times higher than the upper limit; (11) Patients with serum total testosterone levels lower than 25% of the normal limit; (12) Patients who are unwilling or unable to complete their questionnaires.

Design outcomes

Primary

MeasureTime frame
the score of ED domain of the IIF questionnaire(questions1-5, 15);SEP question 2;SEP question 3;

Secondary

MeasureTime frame
comprehensive evaluation questionnaire(GAQ);orgasm score of IIEF questonnarire;sexual satisfaction score in IIEF questionnaire;Overall satisfaction score in IIEF questionnaire;Erectile hardness in SEP patient dairy;sexual in SEP;erection in the morning;

Countries

China

Contacts

Public ContactZhang Zhichao

Peking University First Hospital

zhangzhichao@bjmu.edu.cn+86 13501219421

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026