Depression at 42 days postpartum will be diagnosed by psychiatrists according to the Mini-International Neuropsychiatric Interview (MINI)-6.0.
Low-dose S-ketamine in Women With Prenatal Depression
Brief Summary
Intervention / Treatment
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S-ketamine (DRUG)For women in this group, active drug (s-ketamine 0.2 mg/kg in 20 ml normal saline) will be infused at a rate of 30 ml/h (infusion finished in 40 minutes) after giving birth. They will be monitored for 60 minutes and then sent back to the ward.
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Placebo (DRUG)For women in this group, placebo (20 ml normal saline) will be infused at a rate of 30 ml/h (infusion finished in 40 minutes) after giving birth. They will be monitored for 60 minutes and then sent back to the ward.
Condition or Disease
- Prenatal Depression
- Ketamine
- Postpartum Depression
Phase
Study Design
Study type: | INTERVENTIONAL |
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Status: | Completed |
Study results: | No Results Available |
Age: | 18 Years and older (Adult, Older Adult) |
Enrollment: | 364 (ACTUAL) |
Funded by: | Other |
Allocation: | Randomized |
Primary Purpose: | Prevention |
MaskingQUADRUPLE:
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Clinical Trial Dates
Start date: | Jun 19, 2020 | ACTUAL |
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Primary Completion: | Aug 03, 2022 | ACTUAL |
Completion Date: | Aug 03, 2022 | ACTUAL |
Study First Posted: | Jun 04, 2020 | ACTUAL |
Results First Posted: | Aug 31, 2020 | |
Last Updated: | Apr 01, 2023 |
Sponsors / Collaborators
Participant Groups
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For women in this group, study drug (s-ketamine 0.2 mg/kg in 20 ml normal saline) will be infused at a rate of 30 ml/h (infusion finished in 40 minutes) after giving birth. Women will be monitored for 60 minutes and then sent back to the ward.
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For women in this group, study drug (20 ml normal saline) will be infused at a rate of 30 ml/h (infusion finished in 40 minutes) after giving birth. Women will be monitored for 60 minutes and then sent back to the ward.
Eligibility Criteria
Sex: | Female |
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Minimum Age: | 18 |
Age Groups: | Adult / Older Adult |
Healthy Volunteers: | Yes |
1. Maternal age ≥18 years;
2. Prenatal Edinburgh postnatal depression scale score ≥10 points.
Exclusion Criteria:
1. A clear history of mental illness (depression, schizophrenia, etc.) or communication difficulties;
2. Severe pregnancy complications, such as severe preeclampsia, placental implantation, HELLP (syndrome hemolytic anemia, elevated liver function and low platelet count) syndrom, placenta previa, and placental abruption;
3. American Society of Anesthesiologists classification ≥III;
4. Presence of contraindications to ketamine/s-ketamine use, such as refractory hypertension, severe cardiovascular disease (New York Heart Association classification ≥III), and hyperthyroidism.
Primary Outcomes
Secondary Outcomes
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Maternal depression will be assessed with the Edinburgh Postnatal Depression Scale (EPDS; score range 0-30, with higher score indicating more severe depression). The assessment will be conducted by a telephone interview.
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Maternal depression will be assessed with the Edinburgh Postnatal Depression Scale (EPDS; score range 0-30, with higher score indicating more severe depression). The assessment will be conducted by a face-to-face interview or an online video interview.
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Maternal depression severity will be assessed with the Hamilton Depression Scale-17 (HAMD; score range 0-52, with higher score indicating more severe depression). The assessment will be conducted by a face-to-face interview or an online video interview.
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Intensity of pain will be assessed with the numeric rating scale (a 11-point scale where 0=no pain and 10=the worst pain).
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The mode of baby feeding include breast feeding, mixed feeding, or formula feeding.
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Length of hospital stay after giving birth.
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Maternal complications are defined as those that are harmful to maternal health and require medical intervention.
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Neonatal diseases are defined as those that require medical intervention.
More Details
NCT Number: | NCT04414943 |
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Other IDs: | 2019[336] |
Study URL: | https://clinicaltrials.gov/study/NCT04414943 |