Skip to main content
OpenTrials
Completed

NCT Number: NCT02293694

Sayana® Press Self-injection Study in Malawi

The feasibility of Sayana Press self-injection and the potential for this practice to increase contraceptive continuation has never been assessed in family planning programs in low-resource settings. The Malawi Ministry of Health (MOH) and the United States Agency for International Development (USAID) Malawi Mission requested the Advancing Partners and Communities (APC) project to assess self-injection of Sayana Press to inform their decision-making for procurement of Sayana Press and distribution through the health system in Malawi.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

College of Medicine, Department of Community Health

Blantyre, Malawi

About this study

Sayana® Press is a subcutaneous formulation of depot medroxyprogesterone acetate (DMPA) in a prefilled, auto-disabled injection system called Uniject (Pfizer, Inc., USA). Sayana Press was registered with the Medicines and Health Care Products Regulatory Agency (MHRA) and several other national regulatory agencies. The addition of this method is anticipated to aid in improving provision of family planning services in low-resource settings. As such, Sayana Press could be particularly useful in a country such as Malawi where injectable contraception is the most common method used. DMPA clients and providers are ready to explore the potential of self-injection of Sayana Press. A study conducted in a large family planning clinic in Edinburgh, Scotland found self-administration of DMPA-SC feasible and associated with similar continuation rates and satisfaction to clinician-administered DMPA-IM. A non-comparison study conducted in Planned Parenthood clinics in Florida found continuation of self-injected DMPA-SC high (74%) at the fourth injection. Participants in this study reported the injection to be easy and convenient and were likely to recommend self-administration to other women. Moreover, on September 29, 2014 Pfizer submitted a request to the MHRA to change the Sayana Press label to include self-injection.

If self-injection is found feasible, the results from this research will inform self-injection training materials, messages for providers and clients, and future scale-up efforts in Malawi and elsewhere in sub-Saharan Africa.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Age 18-40, inclusive

  • In general good health (participant verbally reports she feels well)
  • Able to understand and willing to sign an informed consent document
  • Willing to give contact information for follow-up
  • Agree to have follow-up visits/interviews
  • Willing to be randomized to the self-injection arm or provider-administered injection arm
  • Menstrual period started within the past 7 days (for new DMPA users)
  • Meet eligibility criteria for receiving DMPA per WHO Medical Eligibility Criteria (MEC)

Exclusion criteria

Pregnancy

  • Plans to become pregnant in the next 12 months
  • Plans to relocate outside the study area in the next 12 months
  • Any condition (social or medical) which in the opinion of the investigator would make study participation unsafe or would interfere with adherence to study requirements or complicate data interpretation

Treatment and study plan

Sayana Press

Drug

Sayana® Press is a subcutaneous formulation of depot medroxyprogesterone acetate (DMPA) in a prefilled, auto-disabled injection system called Uniject

Other names: depot medroxyprogesterone acetate (DMPA)

Primary outcomes

  1. To compare continuation rates between women who self-inject Sayana Press compared to women who receive Sayana Press injection from a provider

    Time frame: up to 12 months

    Discontinuation of Sayana Press measured at enrollment and every three months through one year

Secondary outcomes

  1. To compare reported side effects between the two study groups

    Time frame: up to 12 months

    Women's reported side effects

  2. To compare pregnancy rates between the two study groups

    Time frame: 12 months

    Frequencies of pregnancies in the two groups reported during the final

Other outcomes

  1. To describe experiences of women who self-inject Sayana Press

    Time frame: 12 months

    Self-injectors' reported experiences (e.g., using, storing, and disposing of Sayana Press)

  2. To describe experiences and recommendations of family planning providers who train women to self-inject Sayana Press

    Time frame: 12 months

    Providers' reported experiences and recommendations

Sponsors and collaborators

Lead sponsor

FHI 360

Other

Registry information

Official study title

A 12-month Open-label Randomized Controlled Trial to Evaluate Sayana® Press Suitability for at Home Subcutaneous Self-injection Procedures in Adult Women

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Nov 18, 2014
Registry last updated
Sep 18, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.