Maternal Hypothermia After Caesarean Section - Implications for Postoperative Recovery

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-50
SponsorOslo University Hospital

About this trial

The aim of the study is to assess patient reported outcomes after caesarean section using self report questionnaire.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Females giving birth through caesarean section

Trial design

Design model

Other

Time perspective

Other

Treatments tested in this trial

  • Self report questionnaire

    Other intervention

    No intervention

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Patient reported recovery after caesarean delivery and symptoms of post caesarean infection

Data collection using questionnaire

Time frame
Data collection 24 hours after surgery and 7 days after surgery and 30 days after surgery

Secondary outcomes

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: