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Naldebain® Extended-release Injection After Cesarean Section in Pain Management

Naldebain® Extended-release Injection After Cesarean Section in Pain Management: a Prospective Observational Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05446311
Enrollment
20
Registered
2022-07-06
Start date
2022-07-15
Completion date
2022-12-31
Last updated
2022-07-06

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

Conditions

Analgesia, Caesarean Section, Post Operative Pain

Keywords

Dinalbuphine Sebacate, NALDEBAIN, Extended-release analgesics

Brief summary

Cesarean section is one of the surgeries most commonly leading to postoperative severe acute pain. It was reported that the mean worst pain intensity reached to 6.14 one day after cesarean section in Germany. Inadequate pain management may result in the cardiorespiratory complications, late recovery, and postoperative chronic pain. According to a series of pain management article published in the Lancent in 2019, the incidence of post-cesarean section chronic pain was 55%, including 12% of severe chronic pain. Extended-release dinalbuphine sebacate, a prodrug of nalbuphine, is a novel analgesic developed in Taiwan and the indication is moderate to severe postoperative pain. After intramuscular injected, dinalbuphine sebacate will be released to blood stream and immediately hydrolyzed. In Taiwan, dinalbuphine sebacate has been used for alleviating pain after several types of surgeries, such as colorectal surgery, orthopaedics, gynecology and obstetrics. However, few post-marketing studies investigated the efficacy and safety of dinalbuphine sebacate.

Detailed description

This is an observational, prospective, single arm study. This study is aimed to investigate the efficacy and safety of dinalbuphine sebacate in subjects undergoing cesarean section. Written informed consent are obtained before subjects participate in the study. Eligible subjects will be visited twice daily during stay in hospital. Pain intensity, consumption of analgesics, adverse reaction, and the residues of dinalbuphine sebacate and nalbuphine in milk will all be analyzed.

Interventions

After giving the birth, subjects are intramuscularly injected with a single dose of 150 mg of dinalbuphine sebacate (DS). DS is a prodrug of nalbuphine. After injeciton, DS are released to blood stream and hydrolyzed immediately. The onset of action is 12 to 24 hours and the analgesic effect can last about 5 to 7 days.

Sponsors

Tri-Service General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

1. Female aged 20 to 45 years. 2. Going to have cesarean section and use dinalbuphine sebacate to alleviate postoperative pain. 3. Cesarean section scheduled between the 34th and 41st week of gestation. 4. ASA I or II. 5. Willing to comply with study protocol and give written informed consent.

Exclusion criteria

1. With contraindication to opioids. 2. Chronic use or abuse of opioids. 3. Underlying disease which contribute to abnormal lactation, such as mastitis. 4. Diagnosed with gestational diabetes mellitus and administration of insulin is required. 5. Diagnosed with pre-eclampsia or eclampsia. 6. Unsuitable for participation judged by investigator.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of complicationWithin 5 days after injection of dinalbuphine sebacateAnalgesic-related complication occurring in the period of hospital stay will be recorded, such as dizziness, nausea, vomiting, and injection site reaction.

Secondary

MeasureTime frameDescription
Post-cesarean section pain intensityWithin 5 days after deliveryPain intensity is assessed by numerical rating scale (NRS) twice daily during stay
Consumption of analgesicsWithin 5 days after deliveryAnalgesics consumed during stay of hospital are recorded.
Concentration of nalbuphine in breast milkWithin 5 days after deliveryDinalbuphine sebacate is a prodrug of nalbuphine. After intramuscular injection, dinalbuphine sebacate are slowly released to blood stream and immediately hydrolyzed. The breast milk is collected twice daily within 5 days after cesarean section, and tested by HPLC.
Concentration of dinalbuphine sebacate in breast milkWithin 5 days after deliveryDinalbuphine sebacate is a prodrug of nalbuphine. After intramuscular injection, dinalbuphine sebacate are slowly released to blood stream and immediately hydrolyzed. The breast milk is collected twice daily within 5 days after cesarean section, and tested by HPLC.

Contacts

Primary ContactChi-Kang Lin, MD
kung568@gmail.com+886-2-87923311

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026