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Clinical outcome of routine treatment of patients with Pelvic Inflammatory Disease and/or Tubo Ovarial Abcess in the presence or absence of Mycoplasma genitalium (MG)

Clinical outcome of routine treatment of patients with Pelvic Inflammatory Disease and/or Tubo Ovarial Abcess in the presence or absence of Mycoplasma genitalium (MG) - Clinical outcome of PID- and TOA-patients with and without MG

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON54533
Enrollment
120
Registered
2020-07-02
Start date
2021-04-01
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

PID

Interventions

None listed

Sponsors

GGD Amsterdam
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Patients with PID or TOA

Exclusion criteria

Exclusion criteria: Pregnancy Hypersensitivity to antibiotics given as standard treatment Not being able to understand information provided in Dutch or English

Design outcomes

Primary

MeasureTime frame
Clinical outcome of PID and/or TOA is based on fever, abdominal pain, cervical leucorrhoea during speculum examination, painful genitalia interna, other clinical signs and CRP.

Secondary

MeasureTime frame
1) The presence and persistence of MG-DNA in vaginal swabs. 2) Antibiotic resistance prevalence in MG positive cases.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)